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Vitamin D status of Hong Kong Chinese infants. 香港华裔婴儿的维生素D状况。
Pub Date : 1989-03-01 DOI: 10.1111/j.1651-2227.1989.tb11074.x
S S Leung, S Lui, R Swaminathan

Vitamin D deficiency is a common nutritional problem of weaning infants in many parts of the world. Hong Kong infants, who are fed with traditional rice-based weaning foods and live in crowded high rise flats, might be expected to suffer from this nutritional problem. Yet a study of 150 bottle fed infants revealed that the vitamin D intake from fortified milk and cereals was more than half of the recommended amount throughout the first 18 months and that the serum 25-OH vitamin D concentration of the infants at 18 months was normal. The effect of sunlight was also evident.

维生素D缺乏症是世界许多地区断奶婴儿普遍存在的营养问题。香港的婴儿吃的是传统的以大米为基础的断奶食品,住在拥挤的高层公寓里,可能会受到这种营养问题的困扰。然而,一项对150名奶瓶喂养婴儿的研究表明,在头18个月里,从强化牛奶和谷物中摄入的维生素D超过了推荐量的一半,18个月时婴儿的血清25-OH维生素D浓度是正常的。阳光的影响也很明显。
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引用次数: 26
Echovirus meningoencephalitis in X-linked hypogammaglobulinemia. 伴有x连锁低γ球蛋白血症的Echovirus脑膜脑炎。
Pub Date : 1989-03-01 DOI: 10.1111/j.1651-2227.1989.tb11082.x
L Van Maldergem, F Mascart, D Ureel, E Jauniaux, W Broeckx, M Vainsel
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引用次数: 9
Reference values of anthropometric measurements in Dutch children. The Oosterwolde Study. 荷兰儿童人体测量的参考值。奥斯特沃尔德研究。
Pub Date : 1989-03-01 DOI: 10.1111/j.1651-2227.1989.tb11075.x
W J Gerver, N M Drayer, W Schaafsma

In the period 1979-1980 the following anthropometric measurements were recorded in 2351 healthy Dutch children from 0-17 years of age: height, weight, sitting height, arm span, lengths of upper-arm, lower-arm and hand, tibial length, foot length, biacromial diameter, biiliacal diameter, and head circumference. Corresponding percentile values were constructed on the basis of normality assumptions, the mean and standard deviation at age t being determined by a cubic spline approximation. The results are compared with other studies and given in the form of growth charts.

在1979-1980年期间,对2351名0-17岁的荷兰健康儿童进行了以下人体测量测量:身高、体重、坐高、臂展、上臂、下臂和手的长度、胫骨长度、脚长、双峰直径、双胆道直径和头围。在正态性假设的基础上构建相应的百分位数,t岁时的均值和标准差由三次样条近似确定。结果与其他研究进行了比较,并以生长图表的形式给出。
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引用次数: 37
Non-tropical pyomyositis in children--with report of severe neurological complications. 儿童非热带性肌炎伴严重神经系统并发症报告
Pub Date : 1989-03-01 DOI: 10.1111/j.1651-2227.1989.tb11085.x
R Brik, J Braun, V Bialik, N Zuckerman, M Berant

Pyomyositis appears to occur rarely in temperate climate areas, compared with the incidence of the disease in the tropics. Three young adults with pyomyositis have previously been described in Israel, two of them were newly arrived Ethiopian immigrants. We report three Israeli children with pyomyositis, who presented initially with nonspecific abdominal pain; in one child the course was complicated by spinal cord compression due to extension of the infected mass into the spinal canal. All three patients attained full recovery after antibiotic therapy and surgical drainage. Computed tomography was most valuable in establishing the diagnosis and defining the extent of the process.

与热带地区的发病率相比,化脓性肌炎似乎很少发生在温带气候地区。以前在以色列曾报道过三名患有脓性肌炎的年轻人,其中两人是新抵达的埃塞俄比亚移民。我们报告了三名患有脓性肌炎的以色列儿童,他们最初表现为非特异性腹痛;在一个孩子的病程是复杂的脊髓压迫,由于受感染的肿块延伸到椎管。3例患者均经抗生素治疗和手术引流后完全恢复。计算机断层扫描在确定诊断和确定病程范围方面最有价值。
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引用次数: 11
Cutis marmorata telangiectatica congenita with terminal transverse limb defects. 先天性毛细血管扩张皮肤伴终末横肢缺损。
Pub Date : 1988-09-01 DOI: 10.1111/j.1651-2227.1988.tb10753.x
U S Björnsdottir, T Laxdal, J Björnsson

We describe a girl with clinical and histopathological manifestations characteristic of Cutis Marmorata Telangiectatica Congenita (CMTC) associated with Terminal Transverse Limb Defects (TTLD). In contrast to previous reports on this rare syndrome, no cutaneous atrophy or aplasia was evident in our patient.

我们描述了一个具有先天性毛细血管扩张性皮肤(CMTC)合并终末横肢缺陷(TTLD)的临床和组织病理学表现特征的女孩。与以往报道的这种罕见综合征相反,我们的患者没有明显的皮肤萎缩或发育不全。
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引用次数: 22
Urinary sodium excretion in diabetic children. 糖尿病儿童尿钠排泄。
Pub Date : 1988-09-01 DOI: 10.1111/j.1651-2227.1988.tb10745.x
A F Hackett, S Court, C McCowen, J M Parkin
L'excretion urinaire de sodium est correlee a divers parametres: sexe, âge, poids, glycosurie, chez des enfants diabetiques
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引用次数: 2
Mineral metabolism in obese children. 肥胖儿童的矿物质代谢。
Pub Date : 1988-09-01 DOI: 10.1111/j.1651-2227.1988.tb10740.x
G Zamboni, M Soffiati, D Giavarina, L Tató

Blood levels of glucose, insulin (IRI), Calcium (Ca), phosphorus (P), alkaline phosphatase (AP), osteocalcin (OC), parathyroid hormone (PTH), calcitonin (CT), 25-hydroxyvitamin D3 (25OHD3), 1,25-dihydroxyvitamin D3 (1,25(OH)2D3) and urinary excretion of Ca (Ca/Cr), P (TmP/GFR), hydroxyproline (OH-P/Cr) and cyclic AMP (cAMP/GFR) were determined in 16 obese children, aged 8 to 11 years, on a diet rich in calories and carbohydrates and in 15 controls of the same age. Blood glucose, IRI, Ca, P, PTH and CT were also determined in both groups of subjects, during an oral glucose tolerance test (OGTT). In basal conditions glucose, IRI, AP, OC, PTH, CT and 1,25(OH)2D3 levels were significantly higher, and 25OHD3 levels lower, in obese children than in controls. Urinary Ca/Cr, TmP/GFR were lower in obese than in non obese children, while OH-P/Cr and cAMP/GFR were higher. Bone mineral content (BMC), measured by photon absorptiometry, and BMC/bone width ratio were lower in obese than in non obese children. During OGTT serum Ca and P decreased and serum PTH and CT increased less in obese than in non obese children. In obese children receiving a diet with high carbohydrate content, an alteration of mineral metabolism occurred, characterized by secondary increase of PTH and 1,25(OH)2D3. Ca decreased and PTH and CT increased less markedly during OGTT.

测定16例8 ~ 11岁肥胖儿童的血糖、胰岛素(IRI)、钙(Ca)、磷(P)、碱性磷酸酶(AP)、骨钙素(OC)、甲状旁腺激素(PTH)、降钙素(CT)、25-羟基维生素D3 (25OHD3)、1,25(OH)2D3)和尿中Ca (Ca/Cr)、P (TmP/GFR)、羟脯氨酸(OH-P/Cr)和环AMP (cAMP/GFR)的水平。在口服糖耐量试验(OGTT)期间,测定两组受试者的血糖、IRI、Ca、P、PTH和CT。在基础条件下,肥胖儿童的血糖、IRI、AP、OC、PTH、CT和125 (OH)2D3水平显著高于对照组,25OHD3水平显著低于对照组。肥胖儿童尿Ca/Cr、TmP/GFR低于非肥胖儿童,OH-P/Cr和cAMP/GFR高于非肥胖儿童。肥胖儿童的骨矿物质含量(BMC)和BMC/骨宽比均低于非肥胖儿童。在OGTT期间,肥胖儿童血清钙、磷下降,血清甲状旁腺素和CT升高低于非肥胖儿童。在接受高碳水化合物饮食的肥胖儿童中,矿物质代谢发生改变,其特征是甲状旁腺激素和125 (OH)2D3的继发性增加。OGTT期间Ca降低,PTH和CT升高不明显。
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引用次数: 36
Thrombocytopenic purpura and coeliac disease. 血小板减少性紫癜和乳糜泻。
Pub Date : 1988-09-01 DOI: 10.1111/j.1651-2227.1988.tb10749.x
L Stenhammar, C G Ljunggren

In a child with immune thrombocytopenic purpura (ITP) the findings of circulating reticulin antibodies and IgA and IgG gliadin antibodies suggested the diagnosis of coeliac disease. This was verified by small intestinal biopsy. In spite of a gluten-free diet the thrombocytopenia persisted. The association of ITP and coeliac disease was previously described in adults but to our knowledge this is the first report of the coexistence of ITP and coeliac disease in a child.

在一个儿童与免疫性血小板减少性紫癜(ITP)的循环网状蛋白抗体和IgA和IgG麦胶蛋白抗体的结果提示乳糜泻的诊断。小肠活检证实了这一点。尽管无麸质饮食,血小板减少症仍然存在。ITP和乳糜泻的关联以前在成人中有过报道,但据我们所知,这是第一次报道ITP和乳糜泻在儿童中共存。
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引用次数: 35
A syndrome of progressive pancytopenia with microcephaly, cerebellar hypoplasia and growth failure. 一种进行性全血细胞减少伴小头畸形、小脑发育不全和生长衰竭的综合征。
Pub Date : 1988-09-01 DOI: 10.1111/j.1651-2227.1988.tb10751.x
S Hreidarsson, K Kristjansson, G Johannesson, J H Johannsson

A male infant with congenital thrombocytopenia, progressing to pancytopenia in the second year of life is presented. Other findings included microcephaly with cerebellar hypoplasia, growth failure of prenatal onset and severe psychomotor retardation. He died at 23 months of age from candida albicans septicemia. Laboratory studies and a postmortem examination failed to reveal any known etiology for his disorder, but parental consanguinity suggests a genetic basis with an autosomal recessive mode of inheritance. Høyeraal et al. have previously reported two brothers with similar clinical and laboratory findings. It is proposed that the condition of these three patients should be considered as a separate syndrome of congenital pancytopenia, distinguished from other congenital myeloid dysplasias by the extramedullary findings.

一个男性婴儿先天性血小板减少症,进展到全血细胞减少症在生命的第二年提出。其他发现包括小头畸形伴小脑发育不全,产前发育失败和严重的精神运动迟缓。他在23个月大时死于白色念珠菌败血症。实验室研究和尸检未能揭示其疾病的任何已知病因,但父母的血缘关系表明其遗传基础为常染色体隐性遗传模式。Høyeraal等人先前报道过两兄弟有类似的临床和实验室结果。我们建议,这3例患者的情况应被视为先天性全血细胞减少症的单独综合征,通过髓外表现与其他先天性髓细胞增生不良症区分开来。
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引用次数: 108
Effect of prophylactic acetaminophen administration on reaction to DTP vaccination. 预防性给药扑热息痛对百白破疫苗接种反应的影响。
Pub Date : 1988-09-01 DOI: 10.1111/j.1651-2227.1988.tb10741.x
M Uhari, J Hietala, M K Viljanen

The effectiveness of acetaminophen in preventing post-vaccination fever was studied in a double-blind randomized manner. Healthy five-month-old infants vaccinated with diphtheria-tetanus-pertussis (DTP) or DTP-inactivated polio vaccine were randomly allocated to receive either placebo (n = 130) or 75 mg of acetaminophen (n = 133) four hours after the vaccination. Rectal temperatures of the infants were measured in the post-vaccination evening and next morning by the parents. The mean values of rectal temperatures were equal in both groups, i.e. 37.6 degrees C, both in the evening and in the morning. No significant difference was found in the occurrence of other minor adverse reactions. Antibody titres to diphtheria and tetanus toxoids and pertussis bacteria of the placebo (n = 25) and acetaminophen (n = 34) groups did not differ significantly from each other. It is concluded that acetaminophen in a single dose schedule is ineffective in decreasing post-vaccination fever and other symptoms.

采用双盲随机方法研究对乙酰氨基酚预防疫苗接种后发热的有效性。接种白喉-破伤风-百日咳(DTP)或DTP灭活脊髓灰质炎疫苗的健康5个月婴儿在接种疫苗4小时后随机分配接受安慰剂(n = 130)或75毫克对乙酰氨基酚(n = 133)。在接种疫苗后的晚上和第二天早上由父母测量婴儿的直肠温度。两组患者的直肠温度平均值均为37.6℃,均在晚上和早上。其他轻微不良反应的发生率无显著差异。安慰剂组(n = 25)和对乙酰氨基酚组(n = 34)对白喉、破伤风类毒素和百日咳细菌的抗体滴度差异无统计学意义。结论:单剂量对乙酰氨基酚对降低疫苗接种后发热等症状无效。
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引用次数: 28
期刊
Acta paediatrica Scandinavica
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