首页 > 最新文献

Acta paediatrica Scandinavica最新文献

英文 中文
Examination of infant brain maturation using ultra low field MRI. 超低场核磁共振检查婴儿脑成熟。
Pub Date : 1988-07-01 DOI: 10.1111/j.1651-2227.1988.tb10692.x
H Suhonen-Polvi, H Määttänen, A Alanen, K Katevuo, A Tenovuo, P Kero, M Kormano

The brains of 42 newborn infants were examined with MRI at 0.02 T field, and regional variations of T1 relaxation time were measured from the images. There were three groups: 1. full term infants (9), 2. preterm infants (10) and 3. SGA (= small for gestational age) infants (20). Relaxation times showed a correlation to myelination of the brain. The brain of SGA infants showed a large variation in their T1 values.

对42例新生儿进行0.02 T场MRI检查,并从图像中测量T1弛豫时间的区域变化。有三组:1;足月婴儿(9),2。早产儿(10岁)和3岁。SGA(小于胎龄)婴儿(20)。放松时间与大脑的髓鞘形成有关。SGA婴儿的大脑T1值变化较大。
{"title":"Examination of infant brain maturation using ultra low field MRI.","authors":"H Suhonen-Polvi,&nbsp;H Määttänen,&nbsp;A Alanen,&nbsp;K Katevuo,&nbsp;A Tenovuo,&nbsp;P Kero,&nbsp;M Kormano","doi":"10.1111/j.1651-2227.1988.tb10692.x","DOIUrl":"https://doi.org/10.1111/j.1651-2227.1988.tb10692.x","url":null,"abstract":"<p><p>The brains of 42 newborn infants were examined with MRI at 0.02 T field, and regional variations of T1 relaxation time were measured from the images. There were three groups: 1. full term infants (9), 2. preterm infants (10) and 3. SGA (= small for gestational age) infants (20). Relaxation times showed a correlation to myelination of the brain. The brain of SGA infants showed a large variation in their T1 values.</p>","PeriodicalId":75407,"journal":{"name":"Acta paediatrica Scandinavica","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1651-2227.1988.tb10692.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14519746","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Estrogen treatment of excessively tall girls with Marfan syndrome. 雌激素治疗高个女孩马凡氏综合征。
Pub Date : 1988-07-01 DOI: 10.1111/j.1651-2227.1988.tb10696.x
J Knudtzon, D Aarskog

Five girls with Marfan syndrome were treated with estrogens for reduction of their final heights. Treatment was started at a chronological age of 12.0 +/- 0.5 years and height of 173.0 +/- 3.1 cm (means +/- SEM). Skeletal age was 12.4 +/- 0.2 years and Bayley-Pinneau final height prediction 186.3 +/- 1.4 cm. Estrogen treatment for 2.0 +/- 0.4 years resulted in final height of 184.1 +/- 0.2 cm (p less than 0.05). The weight increased with 7.8 +/- 2.7 kg during the treatment period. The present results indicate that estrogen treatment may be effective in reducing adult height in girls with Marfan syndrome, but that the effect is probably less than that observed in normally tall girls. This may probably be explained by the rather late start of treatment. No immediate effects on aortic root diameters were observed. Estrogen treatment in Marfan syndrome is discussed with regard to beneficial effects, possible side-effects and optimal age for starting treatment.

5名患有马凡氏综合征的女孩接受雌激素治疗,以降低她们的最终高度。开始治疗时年龄为12.0 +/- 0.5岁,身高为173.0 +/- 3.1 cm(平均+/- SEM)。骨骼年龄12.4 +/- 0.2岁,Bayley-Pinneau预测最终身高186.3 +/- 1.4 cm。雌激素治疗2.0 +/- 0.4年,最终身高为184.1 +/- 0.2 cm (p < 0.05)。处理期间体重增加7.8±2.7 kg。目前的结果表明,雌激素治疗可能有效降低马凡氏综合征女孩的成年身高,但效果可能低于正常身高的女孩。这可能是由于治疗开始得较晚。没有观察到对主动脉根直径的直接影响。讨论了雌激素治疗马凡氏综合征的有益效果,可能的副作用和最佳开始治疗的年龄。
{"title":"Estrogen treatment of excessively tall girls with Marfan syndrome.","authors":"J Knudtzon,&nbsp;D Aarskog","doi":"10.1111/j.1651-2227.1988.tb10696.x","DOIUrl":"https://doi.org/10.1111/j.1651-2227.1988.tb10696.x","url":null,"abstract":"<p><p>Five girls with Marfan syndrome were treated with estrogens for reduction of their final heights. Treatment was started at a chronological age of 12.0 +/- 0.5 years and height of 173.0 +/- 3.1 cm (means +/- SEM). Skeletal age was 12.4 +/- 0.2 years and Bayley-Pinneau final height prediction 186.3 +/- 1.4 cm. Estrogen treatment for 2.0 +/- 0.4 years resulted in final height of 184.1 +/- 0.2 cm (p less than 0.05). The weight increased with 7.8 +/- 2.7 kg during the treatment period. The present results indicate that estrogen treatment may be effective in reducing adult height in girls with Marfan syndrome, but that the effect is probably less than that observed in normally tall girls. This may probably be explained by the rather late start of treatment. No immediate effects on aortic root diameters were observed. Estrogen treatment in Marfan syndrome is discussed with regard to beneficial effects, possible side-effects and optimal age for starting treatment.</p>","PeriodicalId":75407,"journal":{"name":"Acta paediatrica Scandinavica","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1651-2227.1988.tb10696.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14519748","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 16
Orocoecal transit time in healthy and constipated children. 健康儿童和便秘儿童的口腔运输时间。
Pub Date : 1988-07-01 DOI: 10.1111/j.1651-2227.1988.tb10704.x
P Vajro, G Silano, D Longo, A Staiano, A Fontanella

Orocoecal transit time (OCTT), assessed by means of H2 breath test after lactulose and/or after a semisolid standard meal, was studied in normal and constipated children. Both control subjects and patients with constipation showed a significantly longer OCTT after a standard meal than after lactulose ingestion (p less than 0.01). Whereas the OCTT after lactulose did not differ in the two groups, the constipated patients had a significantly longer transit time after a standard meal when compared to controls (p less than 0.05). No correlation was observed within each group between the OCTT after a standard meal or after lactulose ingestion (r = -0.077; p greater than 0.01). These findings suggest that 1) measurement of the transit of a standard meal instead of a lactulose solution may offer more direct insight into the role of small intestinal transit of food, both in physiological and pathological conditions, 2) gastrointestinal segments other than colon may play a role in chronic non organic constipation of childhood.

在正常儿童和便秘儿童中研究了乳果糖和/或半固体标准餐后,通过H2呼气试验评估口肠运输时间(OCTT)。对照组和便秘患者在标准餐后的OCTT均明显长于摄入乳果糖后的OCTT (p < 0.01)。虽然两组服用乳果糖后的OCTT没有差异,但与对照组相比,便秘患者在标准餐后的转运时间明显更长(p < 0.05)。在每组中,标准餐后的OCTT与摄入乳果糖后的OCTT没有相关性(r = -0.077;P > 0.01)。这些发现表明:1)测量一顿标准膳食的输送量,而不是乳果糖溶液,可以更直接地了解食物在生理和病理条件下小肠输送的作用;2)除结肠外的胃肠道部分可能在儿童慢性非器质性便秘中起作用。
{"title":"Orocoecal transit time in healthy and constipated children.","authors":"P Vajro,&nbsp;G Silano,&nbsp;D Longo,&nbsp;A Staiano,&nbsp;A Fontanella","doi":"10.1111/j.1651-2227.1988.tb10704.x","DOIUrl":"https://doi.org/10.1111/j.1651-2227.1988.tb10704.x","url":null,"abstract":"<p><p>Orocoecal transit time (OCTT), assessed by means of H2 breath test after lactulose and/or after a semisolid standard meal, was studied in normal and constipated children. Both control subjects and patients with constipation showed a significantly longer OCTT after a standard meal than after lactulose ingestion (p less than 0.01). Whereas the OCTT after lactulose did not differ in the two groups, the constipated patients had a significantly longer transit time after a standard meal when compared to controls (p less than 0.05). No correlation was observed within each group between the OCTT after a standard meal or after lactulose ingestion (r = -0.077; p greater than 0.01). These findings suggest that 1) measurement of the transit of a standard meal instead of a lactulose solution may offer more direct insight into the role of small intestinal transit of food, both in physiological and pathological conditions, 2) gastrointestinal segments other than colon may play a role in chronic non organic constipation of childhood.</p>","PeriodicalId":75407,"journal":{"name":"Acta paediatrica Scandinavica","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1651-2227.1988.tb10704.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14519753","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 24
Possible etiological factors in extensive periventricular leukomalacia of preterm infants. 早产儿广泛脑室周围白质软化的可能病因。
Pub Date : 1988-07-01 DOI: 10.1111/j.1651-2227.1988.tb10689.x
R S Ikonen, E J Kuusinen, M O Janas, M J Koivikko, A E Sorto

During a twelve-month period five cases of extensive periventricular leukomalacia (PVL) in preterm infants with a gestational age of 31-32 weeks were diagnosed by routine ultrasound screening of preterm infants. The perinatal courses and later development of these infants were compared with 12 other infants with a comparable gestational age born during the same time period. PVL babies were delivered more often by the vaginal route (p = 0.0034), and their mean highest serum total bilirubin value was significantly higher (p = 0.0054) than that of the control infants. The mean value of the highest blood pH during the first 72 hours of life was also significantly higher (p = 0.0311) in PVL babies than in control babies. On the basis of these results we speculate that in addition to ischaemia in the periventricular area, bilirubin toxicity may play an additional role in the severe damage seen in extensive periventricular leukomalacia.

在12个月期间,5例广泛性脑室周围白质软化(PVL)在胎龄31-32周的早产儿诊断常规超声筛查早产儿。将这些婴儿的围产期和后期发育情况与同期出生的其他12名胎龄相当的婴儿进行比较。PVL患儿经阴道分娩较多(p = 0.0034),其平均最高血清总胆红素值显著高于对照组(p = 0.0054)。PVL婴儿出生后72小时内最高血pH值的平均值也显著高于对照组(p = 0.0311)。基于这些结果,我们推测除了脑室周围区域的缺血外,胆红素毒性可能在广泛脑室周围白质软化的严重损害中起额外的作用。
{"title":"Possible etiological factors in extensive periventricular leukomalacia of preterm infants.","authors":"R S Ikonen,&nbsp;E J Kuusinen,&nbsp;M O Janas,&nbsp;M J Koivikko,&nbsp;A E Sorto","doi":"10.1111/j.1651-2227.1988.tb10689.x","DOIUrl":"https://doi.org/10.1111/j.1651-2227.1988.tb10689.x","url":null,"abstract":"<p><p>During a twelve-month period five cases of extensive periventricular leukomalacia (PVL) in preterm infants with a gestational age of 31-32 weeks were diagnosed by routine ultrasound screening of preterm infants. The perinatal courses and later development of these infants were compared with 12 other infants with a comparable gestational age born during the same time period. PVL babies were delivered more often by the vaginal route (p = 0.0034), and their mean highest serum total bilirubin value was significantly higher (p = 0.0054) than that of the control infants. The mean value of the highest blood pH during the first 72 hours of life was also significantly higher (p = 0.0311) in PVL babies than in control babies. On the basis of these results we speculate that in addition to ischaemia in the periventricular area, bilirubin toxicity may play an additional role in the severe damage seen in extensive periventricular leukomalacia.</p>","PeriodicalId":75407,"journal":{"name":"Acta paediatrica Scandinavica","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1651-2227.1988.tb10689.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14520666","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
Bilirubin binding and acid-base equilibrium in newborn infants with low birthweight. 低出生体重新生儿胆红素结合与酸碱平衡。
Pub Date : 1988-07-01 DOI: 10.1111/j.1651-2227.1988.tb10690.x
P Meisel, D Jährig, E Beyersdorff, K Jährig

Acidosis is known as a risk factor for the development of bilirubin encephalopathy in neonatal jaundice. However, few attempts have been made to evaluate the influence of acid-base state on bilirubin-albumin binding state in blood of newborn infants. Therefore, in 171 appropriate and 83 small for gestational age newborns (birthweight less than 2,500 g) the acid-base state in blood and bilirubin (BR) binding state in serum was measured at the ages of 3, 4, 5, and 8 days. There is a weak but significant correlation between standard base deficit and the ratio BR/reserve albumin as well as the toxic potential of serum BR. The results suggest that the higher risk in acidosis is not only caused by increased tissue binding of BR but also--at least partially--attributable to decreased BR binding in serum.

酸中毒被认为是新生儿黄疸中胆红素脑病发展的危险因素。然而,很少有人尝试评估酸碱状态对新生儿血液中胆红素-白蛋白结合状态的影响。因此,在171例适龄新生儿和83例小于胎龄新生儿(出生体重小于2500 g)中,测定了3、4、5和8天时血酸碱状态和血清胆红素(BR)结合状态。标准碱基缺陷与BR/储备白蛋白比值及血清BR的毒性潜势之间存在微弱但显著的相关性。结果表明,较高的酸中毒风险不仅是由BR的组织结合增加引起的,而且-至少部分-可归因于血清中BR结合减少。
{"title":"Bilirubin binding and acid-base equilibrium in newborn infants with low birthweight.","authors":"P Meisel,&nbsp;D Jährig,&nbsp;E Beyersdorff,&nbsp;K Jährig","doi":"10.1111/j.1651-2227.1988.tb10690.x","DOIUrl":"https://doi.org/10.1111/j.1651-2227.1988.tb10690.x","url":null,"abstract":"<p><p>Acidosis is known as a risk factor for the development of bilirubin encephalopathy in neonatal jaundice. However, few attempts have been made to evaluate the influence of acid-base state on bilirubin-albumin binding state in blood of newborn infants. Therefore, in 171 appropriate and 83 small for gestational age newborns (birthweight less than 2,500 g) the acid-base state in blood and bilirubin (BR) binding state in serum was measured at the ages of 3, 4, 5, and 8 days. There is a weak but significant correlation between standard base deficit and the ratio BR/reserve albumin as well as the toxic potential of serum BR. The results suggest that the higher risk in acidosis is not only caused by increased tissue binding of BR but also--at least partially--attributable to decreased BR binding in serum.</p>","PeriodicalId":75407,"journal":{"name":"Acta paediatrica Scandinavica","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1651-2227.1988.tb10690.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13976999","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Non-enzymatic glycation of fetal tissue in diabetic pregnancy. Estimation of the glucitollysine content of umbilical cord extracts. 糖尿病妊娠胎儿组织的非酶糖基化。脐带提取物葡糖赖氨酸含量的测定。
Pub Date : 1988-07-01 DOI: 10.1111/j.1651-2227.1988.tb10687.x
A Pollak, H R Salzer, A Lischka, M Hayde

Non-enzymatic glycation of fetal tissue was studied by determining the glucitollysine content of umbilical cord extracts from twelve infants of diabetic mothers and fourteen infants of healthy, non-diabetic women (controls). The single, glycated amino-acid glycitollysine, which reflects the extent of glycation processes in biological samples, was measured by a standard amino acid ion exchange chromatography followed by reverse phase high pressure liquid chromatography. Infants of diabetic mothers had significantly higher cord glucitollysine levels than infants of control mothers (14.3 + 4.6 vs. 5.5 + 2.1 ng/mg dry tissue; M + SD, p less than 0.001). Moreover, five infants of diabetic mothers with congenital anomalies had strikingly high glucitollysine levels, higher than the mean +4 SD of the controls. We conclude, that non-enzymatic glycation of fetal tissue does occur as a result of an in utero exposure to cumulative glycemia. Major congenital anomalies in diabetic pregnancies are associated with a greater extent of non-enzymatic glycation of umbilical cord tissue.

通过测定12名糖尿病母亲的婴儿和14名健康的非糖尿病妇女的婴儿(对照组)的脐带提取物的葡糖赖氨酸含量,研究了胎儿组织的非酶糖基化。通过标准氨基酸离子交换色谱法和反相高压液相色谱法测定了反映生物样品中糖基化过程程度的单糖基化氨基酸glycitolysine。糖尿病母亲的婴儿脐带糖聚赖氨酸水平明显高于对照组母亲的婴儿(14.3 + 4.6 vs 5.5 + 2.1 ng/mg干组织;M + SD, p < 0.001)。此外,5名患有先天性异常的糖尿病母亲所生的婴儿的糖糖赖氨酸水平显著高,高于对照组的平均值+4 SD。我们的结论是,胎儿组织的非酶糖基化确实是由于子宫内暴露于累积血糖而发生的。糖尿病妊娠的主要先天性异常与脐带组织的非酶糖化程度较大有关。
{"title":"Non-enzymatic glycation of fetal tissue in diabetic pregnancy. Estimation of the glucitollysine content of umbilical cord extracts.","authors":"A Pollak,&nbsp;H R Salzer,&nbsp;A Lischka,&nbsp;M Hayde","doi":"10.1111/j.1651-2227.1988.tb10687.x","DOIUrl":"https://doi.org/10.1111/j.1651-2227.1988.tb10687.x","url":null,"abstract":"<p><p>Non-enzymatic glycation of fetal tissue was studied by determining the glucitollysine content of umbilical cord extracts from twelve infants of diabetic mothers and fourteen infants of healthy, non-diabetic women (controls). The single, glycated amino-acid glycitollysine, which reflects the extent of glycation processes in biological samples, was measured by a standard amino acid ion exchange chromatography followed by reverse phase high pressure liquid chromatography. Infants of diabetic mothers had significantly higher cord glucitollysine levels than infants of control mothers (14.3 + 4.6 vs. 5.5 + 2.1 ng/mg dry tissue; M + SD, p less than 0.001). Moreover, five infants of diabetic mothers with congenital anomalies had strikingly high glucitollysine levels, higher than the mean +4 SD of the controls. We conclude, that non-enzymatic glycation of fetal tissue does occur as a result of an in utero exposure to cumulative glycemia. Major congenital anomalies in diabetic pregnancies are associated with a greater extent of non-enzymatic glycation of umbilical cord tissue.</p>","PeriodicalId":75407,"journal":{"name":"Acta paediatrica Scandinavica","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1651-2227.1988.tb10687.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14266573","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Glycogen storage disease type I and III and pyruvate carboxylase deficiency: results of long-term treatment with uncooked cornstarch. 糖原储存病I型和III型和丙酮酸羧化酶缺乏症:长期用生玉米淀粉治疗的结果。
Pub Date : 1988-07-01 DOI: 10.1111/j.1651-2227.1988.tb10695.x
K Ullrich, H Schmidt, A van Teeffelen-Heithoff
ABSTRACT. Three patients with glycogen storage disease type I (GSD‐I), three with glycogen storage disease type III (GSD‐III) and one with pyruvate carboxylase deficiency (PCD) could be successfully switched over from continuous nocturnal gastric drip feeding (GDF) to nocturnal feeding with uncooked cornstarch in yoghurt or “quark” (CSF) at the age of 4–20 years. The new kind of therapy is much more convenient for the patients. When followed up to 30 months, patients on CSF showed the same clinical and laboratory findings as during the last two years with GDF. CSF was not introduced to three patients with GSD‐I. Two of them refused the permanent starch‐yoghurt meals. In the third patient the morning blood glucose concentrations were too variable.
3例糖原储存病I型(GSD-I)、3例糖原储存病III型(GSD-III)和1例丙酮酸羧化酶缺乏症(PCD)患者在4-20岁时可以成功地从夜间连续滴胃(GDF)改为夜间用未煮熟的酸奶玉米淀粉或“克”(CSF)喂养。这种新疗法对病人来说方便多了。随访30个月后,CSF患者的临床和实验室结果与过去两年的GDF患者相同。3例GSD-I患者未引入CSF。其中两人拒绝了长期的淀粉酸奶餐。第三个病人早上的血糖浓度变化太大。
{"title":"Glycogen storage disease type I and III and pyruvate carboxylase deficiency: results of long-term treatment with uncooked cornstarch.","authors":"K Ullrich,&nbsp;H Schmidt,&nbsp;A van Teeffelen-Heithoff","doi":"10.1111/j.1651-2227.1988.tb10695.x","DOIUrl":"https://doi.org/10.1111/j.1651-2227.1988.tb10695.x","url":null,"abstract":"ABSTRACT. Three patients with glycogen storage disease type I (GSD‐I), three with glycogen storage disease type III (GSD‐III) and one with pyruvate carboxylase deficiency (PCD) could be successfully switched over from continuous nocturnal gastric drip feeding (GDF) to nocturnal feeding with uncooked cornstarch in yoghurt or “quark” (CSF) at the age of 4–20 years. The new kind of therapy is much more convenient for the patients. When followed up to 30 months, patients on CSF showed the same clinical and laboratory findings as during the last two years with GDF. CSF was not introduced to three patients with GSD‐I. Two of them refused the permanent starch‐yoghurt meals. In the third patient the morning blood glucose concentrations were too variable.","PeriodicalId":75407,"journal":{"name":"Acta paediatrica Scandinavica","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1651-2227.1988.tb10695.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14266574","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Antivenom treatment in snake bites. 抗蛇毒血清治疗蛇咬伤。
Pub Date : 1988-07-01 DOI: 10.1111/j.1651-2227.1988.tb10707.x
V Curro, A Stabile, V Michetti
{"title":"Antivenom treatment in snake bites.","authors":"V Curro,&nbsp;A Stabile,&nbsp;V Michetti","doi":"10.1111/j.1651-2227.1988.tb10707.x","DOIUrl":"https://doi.org/10.1111/j.1651-2227.1988.tb10707.x","url":null,"abstract":"","PeriodicalId":75407,"journal":{"name":"Acta paediatrica Scandinavica","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1651-2227.1988.tb10707.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14519735","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
The association of supernumerary microtubules and immotile cilia syndrome and defective neutrophil chemotaxis. 多余微管和静止纤毛综合征与中性粒细胞趋化性缺陷的关系。
Pub Date : 1988-07-01 DOI: 10.1111/j.1651-2227.1988.tb10712.x
M Canciani, E G Barlocco, G A Cazzola, G Mastella, M M de Santi, C Gardi, G Lungarella
Several ciliary defects are associated with poor motility or immotility of respiratory cilia. The defects include abnormalities in the axonemal structures or in the basal apparatus (1). Patients suffering from immotile cilia syndrome (ICS) show a heterogeneous clinical disease in which respiratory symptoms (viz. bronchiectasis, chronic bronchitis, otitis media) related to the ciliary dysfunction may be associated with other pathological conditions (i.e. situs viscerum inversus and male infertility). Even if numerous studies in humans and in experimental animals provide more information to explain, a t molecular level, the association between ICS and the above mentioned pathological states, to date, the association between ICS and a defective neutrophil chemotaxis is still object of debate (2). This report deals with four unrelated female patients (aged from 7 to 20 years) suffering from ICS in which a peculiar defect in ciliary configuration was found to be associated with a defective neutrophil chemotaxis. ICS was diagnosed by studying the mucociliary clearance and by examining the ultrastructural morphology of nasal cilia. Nasal mucociliary clearance time was tested by the saccharin method, measuring the time between placing saccharin (1 mm diameter particle) on the inferior turbinate and the moment when the subject tasted its sweetness on swallowing (3). Neutrophil chemotaxis was assessed, in symptom-free periods, “in vivo” and “in vitro” according to Senn (4) and Wilkinson ( 5 ) , respectively. In all patients immunological data were normal, whereas “in vivo” (36.1-17.6-15.9-16.1 x 10’ cells/cm2/24 h; normal values 68+ 10) and “in vitro” (chemotactic index: 121-123-119-1 13; normal values 145+ 11) neutrophil chemotaxis was impaired. The saccharin test (two or more different evaluations for each subject) was abnormal in all patients. In particular the clearance time (reference values 8-30 min) was >60 min in 3 patients, and about 50 min in one of the patients (50-52-55 min). The ultrastructural examination of respiratory cilia showed in all patients the presence of additional solitary peripheral microtubules outside or inside the 9+2 complex (Fig. 1). Cilia with axonemal supernumerary microtubules are reported to be associated to a ciliary dyskinesia (actually those cilia are classified as type V dyskinetic cilia) (1). Although data reported by several authors showed that an impairment of neutrophil chemotaxis is not a constant feature in ICS, the data presented here strongly suggest that a defective neutrophil
{"title":"The association of supernumerary microtubules and immotile cilia syndrome and defective neutrophil chemotaxis.","authors":"M Canciani,&nbsp;E G Barlocco,&nbsp;G A Cazzola,&nbsp;G Mastella,&nbsp;M M de Santi,&nbsp;C Gardi,&nbsp;G Lungarella","doi":"10.1111/j.1651-2227.1988.tb10712.x","DOIUrl":"https://doi.org/10.1111/j.1651-2227.1988.tb10712.x","url":null,"abstract":"Several ciliary defects are associated with poor motility or immotility of respiratory cilia. The defects include abnormalities in the axonemal structures or in the basal apparatus (1). Patients suffering from immotile cilia syndrome (ICS) show a heterogeneous clinical disease in which respiratory symptoms (viz. bronchiectasis, chronic bronchitis, otitis media) related to the ciliary dysfunction may be associated with other pathological conditions (i.e. situs viscerum inversus and male infertility). Even if numerous studies in humans and in experimental animals provide more information to explain, a t molecular level, the association between ICS and the above mentioned pathological states, to date, the association between ICS and a defective neutrophil chemotaxis is still object of debate (2). This report deals with four unrelated female patients (aged from 7 to 20 years) suffering from ICS in which a peculiar defect in ciliary configuration was found to be associated with a defective neutrophil chemotaxis. ICS was diagnosed by studying the mucociliary clearance and by examining the ultrastructural morphology of nasal cilia. Nasal mucociliary clearance time was tested by the saccharin method, measuring the time between placing saccharin (1 mm diameter particle) on the inferior turbinate and the moment when the subject tasted its sweetness on swallowing (3). Neutrophil chemotaxis was assessed, in symptom-free periods, “in vivo” and “in vitro” according to Senn (4) and Wilkinson ( 5 ) , respectively. In all patients immunological data were normal, whereas “in vivo” (36.1-17.6-15.9-16.1 x 10’ cells/cm2/24 h; normal values 68+ 10) and “in vitro” (chemotactic index: 121-123-119-1 13; normal values 145+ 11) neutrophil chemotaxis was impaired. The saccharin test (two or more different evaluations for each subject) was abnormal in all patients. In particular the clearance time (reference values 8-30 min) was >60 min in 3 patients, and about 50 min in one of the patients (50-52-55 min). The ultrastructural examination of respiratory cilia showed in all patients the presence of additional solitary peripheral microtubules outside or inside the 9+2 complex (Fig. 1). Cilia with axonemal supernumerary microtubules are reported to be associated to a ciliary dyskinesia (actually those cilia are classified as type V dyskinetic cilia) (1). Although data reported by several authors showed that an impairment of neutrophil chemotaxis is not a constant feature in ICS, the data presented here strongly suggest that a defective neutrophil","PeriodicalId":75407,"journal":{"name":"Acta paediatrica Scandinavica","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1651-2227.1988.tb10712.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14519737","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 12
Congenital hypothyroid goiter and amiodarone. 先天性甲状腺功能减退和胺碘酮。
Pub Date : 1988-07-01 DOI: 10.1111/j.1651-2227.1988.tb10717.x
D De Wolf, J De Schepper, H Verhaaren, M Deneyer, J Smitz, L Sacre-Smits

Amiodarone is an anti-arrhythmic drug with a content of 39% Iodine. No adverse effects on fetal thyroid function have previously been observed with maternal ingestion of Amiodarone during pregnancy. A case of severe congenital hypothyroidism with goiter, associated with maternal ingestion of 200 mg Amiodarone daily from the 13th week of pregnancy, is described here. No other environmental causes of goiter, nor a congenital organic thyroid disorder could be demonstrated.

胺碘酮是一种抗心律失常药物,碘含量为39%。以前没有观察到孕妇在怀孕期间摄入胺碘酮对胎儿甲状腺功能的不良影响。重度先天性甲状腺功能减退伴甲状腺肿大的病例,与孕妇从妊娠第13周开始每日摄入200毫克胺碘酮有关。没有其他环境原因甲状腺肿,也没有先天性器质性甲状腺疾病可以证明。
{"title":"Congenital hypothyroid goiter and amiodarone.","authors":"D De Wolf,&nbsp;J De Schepper,&nbsp;H Verhaaren,&nbsp;M Deneyer,&nbsp;J Smitz,&nbsp;L Sacre-Smits","doi":"10.1111/j.1651-2227.1988.tb10717.x","DOIUrl":"https://doi.org/10.1111/j.1651-2227.1988.tb10717.x","url":null,"abstract":"<p><p>Amiodarone is an anti-arrhythmic drug with a content of 39% Iodine. No adverse effects on fetal thyroid function have previously been observed with maternal ingestion of Amiodarone during pregnancy. A case of severe congenital hypothyroidism with goiter, associated with maternal ingestion of 200 mg Amiodarone daily from the 13th week of pregnancy, is described here. No other environmental causes of goiter, nor a congenital organic thyroid disorder could be demonstrated.</p>","PeriodicalId":75407,"journal":{"name":"Acta paediatrica Scandinavica","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1651-2227.1988.tb10717.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14519741","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 55
期刊
Acta paediatrica Scandinavica
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1