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Novel mutation in SPTA 1 gene associated with severe hemolytic anemia 与严重溶血性贫血相关的spta1基因新突变
Pub Date : 2018-10-29 DOI: 10.15406/jpnc.2018.08.00351
James R. Polega, Jennifer Stumph, A. Agarwal, Chi Braunreiter
Hereditary spherocytosis (HS), hereditary elliptocytosis (HE), and hereditary pyropoikilocytosis (HPP) are caused by mutations in five genes ANK1, SLC4A1, SPTA1, SPTB and EPB4 which encode for the erythrocyte cytoskeletal proteins, ankyrin, band 3, α-spectrin, β-spectrin and protein 4.2, respectively.1 These mutations and the resultant defective proteins lead to loss of red cell membrane surface area and reduced red cell deformity.2 Approximately 25% of patients will not have a clear family history.3 These autosomal recessive or de novo cases of severe hemolytic anemia pose a diagnostic challenge. We report a pediatric case of hemolytic anemia without a family history, where molecular diagnostics provided a definitive diagnosis of a red cell membrane disorder. The results of the molecular diagnostics demonstrated a complex set of mutations, including a novel mutation in the SPTA1 gene, which assisted in counseling his parents that childhood immunizations and splenectomy would be the appropriate treatment.
遗传性球形细胞增多症(HS)、遗传性椭圆细胞增多症(HE)和遗传性焦样细胞增多症(HPP)是由红细胞细胞骨架蛋白、锚蛋白、带3、α-spectrin、β-spectrin和蛋白4.2编码基因ANK1、SLC4A1、SPTA1、SPTB和EPB4突变引起的这些突变和由此产生的缺陷蛋白导致红细胞表面面积的减少和红细胞变形的减少大约25%的患者没有明确的家族史这些常染色体隐性或新发病例严重溶血性贫血提出了诊断挑战。我们报告一个没有家族史的儿童溶血性贫血病例,其中分子诊断提供了明确的红细胞膜疾病诊断。分子诊断的结果显示了一系列复杂的突变,包括SPTA1基因的新突变,这有助于向他的父母咨询,儿童免疫和脾切除术将是合适的治疗方法。
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引用次数: 0
Review of pressure ulcers management in pediatrics: assessment, prevention, and intervention 儿科压疮管理综述:评估、预防和干预
Pub Date : 2018-10-24 DOI: 10.15406/JPNC.2018.08.00350
H. Sarsak
A Pressure Ulcer (PU) is defined by the National Pressure Ulcer Advisory Panel (NPUAP) as a ‘‘localized injury to the skin and/ or underlying tissue usually over a bony prominence, as a result of pressure, or pressure in combination with shear and/or friction.1 Pus represent a significant healthcare problem and play a critical role in the patients’ quality of life and their treatments affect the patients’ lives emotionally, mentally, physically and socially.2 The staging system of PU was defined by Shea in 1975 and provides a name to the amount of anatomical tissue loss. The original definitions were confusing to many clinicians and lead to inaccurate staging of ulcers associated or due to perineal dermatitis and those due to deep tissue injury. In 2007, the proposed definitions were refined by the NPUAP and described in details with input from an on-line evaluation of their face validity, accuracy clarity, succinctness, utility, and discrimination.1,3
压疮(PU)被国家压疮咨询小组(NPUAP)定义为“由于压力或压力与剪切和/或摩擦相结合,通常在骨突出部位的皮肤和/或底层组织的局部损伤”脓肿是一个重要的健康问题,对患者的生活质量起着至关重要的作用,其治疗影响着患者的情绪、精神、身体和社会生活1975年Shea定义了PU的分期系统,并为解剖组织损失的数量提供了一个名称。最初的定义使许多临床医生感到困惑,并导致与会阴皮炎相关或由会阴皮炎引起的溃疡和由深层组织损伤引起的溃疡的不准确分期。2007年,NPUAP对提出的定义进行了改进,并对其面部效度、准确性、清晰度、简洁性、实用性和区别性的在线评估进行了详细描述
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引用次数: 3
Retrograde intussusception and Giant Meckel’s diverticulum: a rare occurrence in Waugh’s syndrome 逆行性肠套叠及巨型梅克尔憩室:罕见见于沃氏综合征
Pub Date : 2018-10-17 DOI: 10.15406/jpnc.2018.08.00349
Sunita Singh, Intezar Ahmed, J. Rawat
Intussusception is defined as telescoping of proximal bowel segment into immediately adjacent distal bowel segment. Thorek and Lorrimer broadly classified intussusception into ante grade and retrograde variants (Table 1).1 Retrograde/ anti peristaltic/ reverse intussusception (RINT) is defined as “anti peristaltic telescoping of distal bowel into proximal bowel.1,2 Usually RINT occurs in patients with Roux-en-Y gastric bypass, long intestinal tubes, metastatic bowel malignancy, and Achalasia Cardia etc.1−7 Here, we describe a case of ileo-ileal RINT predisposed by a giant Meckel’s diverticulum (MD) in a patient with Waugh’s syndrome..
肠套叠的定义是将近端肠段伸缩到紧邻的远端肠段中。Thorek和Lorimer将肠套叠大致分为前级和逆行型(表1)。1逆行/抗蠕动/反向肠套叠(RINT)定义为“远端肠向近端肠的抗蠕动伸缩。1,2通常RINT发生在Roux-en-Y胃旁路、长肠管、转移性肠恶性肿瘤和贲门失弛缓症等患者中。1−7在此,我们描述了一例因沃氏综合征患者的巨大Meckel憩室(MD)而易发的回肠-回肠RINT。。
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引用次数: 1
Characteristics of rickets in a referral hospital in Khartoum-Sudan 喀土穆-苏丹一家转诊医院的佝偻病特征
Pub Date : 2018-10-10 DOI: 10.15406/JPNC.2018.08.00348
Eltayeb Mohamed Ahmed Tayrab, Mohammed Abbas, Jowayria E Tayrab, K. Mohamed, A. Salih
Rickets is a disease associated with failure of mineralization of growing bones in children.1,2 Rickets may be associated with growth retardation, muscle weakness, hypocalcaemia and alopecia totalis3. Rickets results from defective metabolism of calcium, phosphorus and/or vitamin D.4,5,6 Calcium and vitamin D are important nutrients for skeletal growth and bone health.7 Rickets can be caused by nutritional deficiencies or genetic disorders.4 Nutritional rickets is a health problem in developing countries.8 The most common cause of rickets is vitamin D deficiency.1 Genetic rickets; mostly resulted from mutations in the vitamin D receptor gene.3,9 Active vitamin D has an important role in calcium regulation and bone metabolism.10 Children are particularly vulnerable to 25-hydroxyvitamin D deficiency.7 Vitamin D regulates skeletal homeostasis both indirectly and directly.11 Nutritional type rickets is a child health problem in developing countries.5 Rickets is common among children with severe acute malnutrition and it is associated with increased risks of severe pneumonia and death.12 Vitamin D deficiency with or without calcium deficiency may lead to nutritional rickets.7 Vitamin D; can be synthesized in the skin or absorbed from the diet.11 Renal disorders also effect on mineralization and may be associated with rickets.1 Generally, clinical presentation of the rickets is heterogeneous and includes bone pain and deformities, muscle weakness, short stature and profound sweating.4,2 Rickets increases children susceptibility to infectious diseases.11 There is an association between rickets and some infectious diseases like hematogenous osteomyelitis in children.13 In the differential diagnosis of different forms of rickets; the detailed family history, physical examination, biochemical assessment and X-ray imaging are required.11,2 This study aimed to find the characteristics of rickets at JafarIbn Auf pediatric hospital in Sudan.
Rickets是一种与儿童生长中骨骼矿化失败有关的疾病。1,2 Rickets可能与生长迟缓、肌无力、低钙血症和脱发有关3。软骨病是由钙、磷和/或维生素D代谢缺陷引起的。4,5,6钙和维生素D是骨骼生长和骨骼健康的重要营养素。7软骨病可能由营养缺乏或遗传疾病引起。4营养性软骨病是发展中国家的一个健康问题。8软骨病最常见的原因是维生素D缺乏。1遗传性软骨病;主要是由维生素D受体基因突变引起的。3,9活性维生素D在钙调节和骨代谢中起着重要作用。10儿童特别容易受到25-羟基维生素D缺乏症的影响。7维生素D间接和直接调节骨骼稳态。11营养型软骨病是发展中国家的一个儿童健康问题患有严重急性营养不良的儿童,这与严重肺炎和死亡的风险增加有关。12维生素D缺乏,无论是否缺钙,都可能导致营养性软骨病。7维生素D;可在皮肤中合成或从饮食中吸收。11肾脏疾病也会影响矿化,并可能与软骨病有关。1通常,软骨病的临床表现是异质性的,包括骨痛和畸形、肌肉无力,身材矮小,大汗淋漓。4,2软骨病会增加儿童对传染病的易感性。11软骨病与一些传染病(如儿童血源性骨髓炎)之间存在关联。13在不同形式软骨病的鉴别诊断中;需要详细的家族史、体格检查、生化评估和X射线成像。11,2本研究旨在了解苏丹JafarIbn-Auf儿科医院软骨病的特征。
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引用次数: 1
Assessment of quality of counselling for down syndrome in Sudan 苏丹唐氏综合症咨询质量评估
Pub Date : 2018-10-10 DOI: 10.15406/JPNC.2018.08.00347
Osama Hafiz El Shazali, Hala Abdullahi, H. Osman
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引用次数: 4
Assessment of mother’s knowledge on importance and need for Child Car Safety Seat in UAE 阿拉伯联合酋长国母亲对儿童汽车安全座椅重要性和需求知识的评估
Pub Date : 2018-10-04 DOI: 10.15406/jpnc.2018.08.00360
M. Elhalik, K. El-Atawi, R. Mahfouz, D. D’souza, M. Ali
Automobile-related accidents are one of the prime reasons for morbidity and mortality in infants and children worldwide accounting for 22.3% of the total.1 Lowand middle-income countries have the highest incidences of road accidents worldwide causing 96% of the child deaths. Although United Arab Emirates (UAE) is a high-income country, the prevalence of child fatalities due to road accidents is more than twice of the global projection.2 Every two out of three deaths (~63%) in children below 14 years of age is due to road accidents in UAE.2 Infants taken in arms and child held on lap while driving is vulnerable to get severely injured in case of an accident.3 Restraining child by proper application of seat belts is the sole useful measure for decreasing the number of deaths and disabilities in infants and children due to road accidents.4 Child car safety seat correctly positioned in the back seat of the car along with age-appropriate accessories such as booster seats and lap belt decreases the risk of death and severe injuries in infants by 71% and in children between age 14 years by 54% to 80%.5,6 An inappropriately installed child car safety seat increases the risk of head injuries in children by four times.7 Further, children sitting freely in the rear seat of the motor vehicle experience 35% less of injuries than those in the front.8 To the above situation, an addition of seat belts further decreases the chance of getting injured by 44%.4 This, in turn, lowers the number of hospital admissions in children aged ≤4 years by 69%.9 Nonetheless, Emirati parents remain skeptical about the potency of child car safety seat as evident from their less usage. A preliminary survey conducted by UAE University demonstrated that a child is safer in the arms of the mother was the prevalent misconception among the UAE parents. Moreover, the study also indicated that Emirati parents found inconvenient to use the child safety seat which caused only 20% usage of car safety seats.10 Besides, other hurdles that come in the way of using child car safety seat includes big Emirati family size, Emirati culture, embarrassments felt by the child, and a shortage of police on roads as well as the use of tinted glass by the motorist affecting law enforcement. Albeit numerous initiatives were undertaken for promoting usage of child car safety seat in UAE none are fruitful enough to bring down the child-related fatalities at par with other high-income countries like the USA and Europe.11–14 In USA and Europe, motor vehicle-related child deaths due to road accidents account for only 3% and 5.2% of the total respectively.6 The reason is the lack of use of child safety seat by UAE parents. Among parents, mothers are very concerned about the safety of the infant/child.15 Understanding their awareness and perspective on child safety seat might aid in formulating laws and/or practices
与汽车有关的事故是全世界婴儿和儿童发病和死亡的主要原因之一,占总数的22.3%低收入和中等收入国家是世界上道路交通事故发生率最高的国家,造成96%的儿童死亡。虽然阿拉伯联合酋长国(阿联酋)是一个高收入国家,但道路交通事故造成的儿童死亡发生率是全球预测的两倍多在阿联酋,14岁以下儿童的死亡人数中,每3人中就有2人(约63%)死于交通事故。2在发生事故时,抱在怀里的婴儿和抱在腿上的儿童很容易受到严重伤害3 .正确使用安全带约束儿童是减少因道路交通事故造成的婴儿和儿童死亡和残疾人数的唯一有效措施正确放置在汽车后座上的儿童汽车安全座椅以及与年龄相适应的附件,如增高座椅和安全带,可将婴儿死亡和严重伤害的风险降低71%,将14岁以下儿童的死亡和严重伤害风险降低54%至80%。儿童汽车安全座椅安装不当会使儿童头部受伤的风险增加四倍而且,自由地坐在汽车后座上的孩子比坐在前排的孩子少受35%的伤害对于上述情况,增加安全带可以进一步降低44%的受伤几率这反过来又使4岁以下儿童的住院人数减少了69%尽管如此,阿联酋的父母仍然对儿童汽车安全座椅的效力持怀疑态度,这一点从他们较少使用的情况中可以看出。阿联酋大学进行的一项初步调查显示,“孩子在妈妈怀里更安全”是阿联酋父母普遍存在的误解。此外,该研究还表明,阿联酋父母发现使用儿童安全座椅不方便,这导致只有20%的人使用汽车安全座椅此外,使用儿童汽车安全座椅的其他障碍包括阿联酋的大家庭、阿联酋的文化、孩子感到的尴尬、道路上警察的短缺以及司机使用有色玻璃影响执法。尽管为促进儿童汽车安全座椅的使用在阿联酋采取了许多举措,但没有一项卓有成效,足以将与儿童有关的死亡率降低到与美国和欧洲等其他高收入国家相当的水平。11 - 14在美国和欧洲,由于道路交通事故导致的与机动车辆有关的儿童死亡分别仅占总数的3%和5.2%原因是阿联酋父母缺乏使用儿童安全座椅。在父母中,母亲非常关心婴儿/孩子的安全了解他们对儿童安全座椅的认识和看法可能有助于制定法律和/或实践
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引用次数: 4
Immersive learning as an assessment and training tool for cardiopulmonary resuscitation skills 沉浸式学习作为评估和培训心肺复苏技能的工具
Pub Date : 2018-09-25 DOI: 10.15406/JPNC.2018.08.00345
I. Gavryutina, B. Blokhin
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引用次数: 0
Assessment of newborns at birth for cardio-respiratory status requiring resuscitation and outcomes in a community hospital 社区医院新生儿出生时需要复苏的心肺状况及结果评估
Pub Date : 2018-09-24 DOI: 10.15406/jpnc.2018.08.00344
Sun, T. Zahouani, Olga Brea, Wallis Tavarez, Upma Suneja, B. Rajegowda
neonatal medicine, the rate of hypoxic ischemia continues to be at a constant with an incidence of 2-3 per 1000 live births in USA. HIE is a major cause of morbidity and mortality in term newborns infants.2 HIE has long term outcomes including cerebral palsy. Novel approaches like selective head and whole body cooling have become a standard of care to protect the brain from reperfusion injury, thereby improving their clinical outcome.3
新生儿医学,低氧缺血率继续保持在一个恒定的发生率为2-3每1000活产在美国。HIE是足月新生儿发病和死亡的主要原因HIE的长期后果包括脑瘫。选择性头部和全身冷却等新方法已成为保护大脑免受再灌注损伤的标准治疗方法,从而改善了其临床效果
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引用次数: 0
Carbamyol phosphate synthetase 1 gene (4217C>A) polymorphism and its relation to low plasma arginine level among preterm with necrotizing enterocolitis; a single center Egyptian study Carbamyol磷酸酯合成酶1基因(4217C>A)多态性及其与坏死性小肠结肠炎早产儿血浆精氨酸水平低的关系;单中心埃及研究
Pub Date : 2018-09-18 DOI: 10.15406/JPNC.2018.08.00343
Wesam A. Mokhtar, Reem Mohamed Allam, N. Zidan, Ghada Abdelmonem Mokhtar, M. Hamed
Necrotizing entero-colitis [NEC] is the most prevailing and devastating acquired gastrointestinal emergency among premature neonates.1 Despite the observable worthy advancement in the care of small preemies over the foregoing decades, NEC; as yet; exists as a foremost leading predisposition for as certainable increase in mortality and poor outcome among tiny preemies in neonatal intensive-care-units [NICU].2 Although numerous predisposing factors have been well-settled, the explicit patho-etiological mechanisms of NEC is still unclear. It has been emphasized that the combination of immaturity & underdevelopment of intestinal motility, digestive ability, intestinal barriers, immune defense and intestinal microcirculatory regulation with an abnormal intestinal microbial colonization in the presence of genetic predisposition were the probable patho-etiological predispositions for development of NEC.1,3 Nitric oxide (NO); which is synthesized from amino acid (L-arginine) by NO synthetase enzyme (NOS); is the principle inhibitory neurotransmitter in the gastro-intestinal system. It has a crucial role in maintaining the vasodilator tone, regulate mucosal blood flow, and maintain intestinal mucosal integrity and barrier function. 4,5 L-arginine, which is declared as a functionally essential amino-acid, is one of the urea-cycle intermediates that produced by the action of carbamyol-phostphate synthetase 1(CPS1) enzyme.6 It has been noticed that the unavailability of L-arginine was associated with limitation in NO production and increased predisposition to NEC. In addition, numerous studies disclosed that plasma arginine concentration was declined in preemies with NEC.7–9 Moreover, it has been disclosed that arginine supplementation decreases the liability for NEC development.[7] CPS1 enzyme; which is encoded by CPS1 gene on chromosome (2q34); is the rate-limiting enzyme catalyzing
坏死性肠结肠炎(NEC)是早产儿中最常见和最具破坏性的获得性胃肠道急症尽管在过去的几十年里,在照顾小早产儿方面取得了值得观察的进步,NEC;到目前为止;在新生儿重症监护病房[NICU]中,存在作为死亡率增加和预后不良的首要易感因素虽然许多易感因素已经确定,但NEC的明确病理病因机制仍不清楚。研究强调,肠道运动、消化能力、肠道屏障、免疫防御和肠道微循环调节的不成熟和发育不全,加上肠道微生物定植异常,存在遗传易感性,可能是nec发生的病机易感性。由氨基酸(l -精氨酸)由NO合成酶(NOS)合成;是胃肠道系统中主要的抑制性神经递质。它在维持血管舒张张力、调节粘膜血流量、维持肠粘膜完整性和屏障功能等方面具有至关重要的作用。4、5 l-精氨酸是一种功能性必需氨基酸,是尿素循环的中间体之一,由氨基戊醇-磷酸合成酶1(CPS1)产生人们已经注意到,l -精氨酸的缺乏与一氧化氮产生的限制和NEC易感性的增加有关。此外,大量研究表明,患有NEC的早产儿血浆精氨酸浓度下降。此外,有研究表明,补充精氨酸可以降低NEC发展的风险CPS1酶;由染色体(2q34)上的CPS1基因编码;限速酶有催化作用吗
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引用次数: 0
Superior mesenteric artery syndrome (Wilkie’s syndrome): acute severe presentation in a 10 year old boy and role of early surgical management 肠系膜上动脉综合征(Wilkie's综合征):一名10岁男孩的急性严重表现和早期手术治疗的作用
Pub Date : 2018-09-12 DOI: 10.15406/JPNC.2018.08.00342
Rajat Piplani, S. Acharya, D. Bagga
Superior mesenteric artery syndrome is an atypical condition which was first described in 1861 by von Rokitansky.1 It is an unusual form of upper GI obstruction, also synonymous with Wilkie’s syndrome or cast syndrome or arteriomesenteric duodenal compression or chronic duodenal ileus which occurs due to compression of the third part of duodenum between abdominal aorta posteriorly and superior mesenteric artery anteriorly.2,3 It is mostly due to loss of retroperitoneal fat that normally acts as cushion around the SMA. Patient usually presents with chronic intermittent pain abdomen, bilious vomiting, nausea, early satiety and anorexia. A history of weight loss is usually seen but it is not a necessity.3 The diagnosis is basically by exclusion of other causes of upper GI obstruction and confirmed by upper gastrointestinal contrast study and contrast enhanced CT abdomen. A trial of initial conservative management can be given to all patients but surgical intervention in the form of duodenojejunostomy gives early and complete relief of the symptoms.
肠系膜上动脉综合征是一种非典型疾病,由von rokitansky于1861年首次描述。它是上消化道梗阻的一种不寻常形式,也与Wilkie综合征或cast综合征或十二指肠动脉-肠系膜压迫或慢性十二指肠肠梗阻同义,其发生是由于位于腹主动脉后方和肠系膜上动脉前部之间的十二指肠第三部分受到压迫。这主要是由于腹膜后脂肪的损失,而腹膜后脂肪通常在SMA周围起缓冲作用。患者通常表现为慢性间歇性腹痛、胆汁性呕吐、恶心、早饱和厌食。减肥的历史通常是可见的,但这不是必须的诊断基本排除其他上消化道梗阻原因,经上消化道造影及腹部增强CT证实。所有患者都可以进行初步的保守治疗,但手术干预以十二指肠空肠吻合术的形式可以早期完全缓解症状。
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引用次数: 0
期刊
Journal of pediatrics & neonatal care
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