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نوع الوثيقة : مقال في مجلة دورية 
عنوان الوثيقة :
مرض النيمان بيك فى 30 حالة .
Nova Scotia Niemann-Pick Disease (Type D): Clinical Study of 20 Cases.
 
لغة الوثيقة : الانجليزية 
المستخلص : Patients with Niemann-Pick type D have been traced to a single Acadian ancestor in Nova Scotia. The objective of this study was to describe the clinical course. A cohort of children with Niemann-Pick type D was identified by chart review. Some children were seen and a telephone interview with the remaining parents was conducted. Twenty children with Niemann-Pick type D were identified. The female to male ratio was 2:1. Five children had severe neonatal jaundice. Early milestones were normal in the majority. Neurologic symptoms generally developed between 5 and 10 years of age with a mean age of 7.2 years at diagnosis. Seizures developed in all between 4.5 and 16 years of age (mean, 10.5 yr), and were followed by significant physical and mental deterioration. The age at death ranged between 11 and 22.5 years (mean, 14.8 yr). In 61%, bronchopneumonia was the cause of death. There is significant variability in the presentation and clinical course of Niemann-Pick type D. 
ردمد : 0930-2794 
اسم الدورية : Journal of Child Neurology 
المجلد : 1 
العدد : 13 
سنة النشر : 1998 هـ
1998 م
 
نوع المقالة : مقالة علمية 
تاريخ الاضافة على الموقع : Saturday, March 13, 2010 

الباحثون

اسم الباحث (عربي)اسم الباحث (انجليزي)نوع الباحثالمرتبة العلميةالبريد الالكتروني
محمد جانjan, Mohammed باحثدكتوراه 

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اسم الملفالنوعالوصف
 25947.doc doc 

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