Joubert syndrome with nephronophthisis in neurofibromatosis type 1

المؤلفون المشاركون

Ghamidi, Jawad Ahmad
Ali, Uma S.

المصدر

Saudi Journal of Kidney Diseases and Transplantation

العدد

المجلد 22، العدد 4 (31 أغسطس/آب 2011)، ص ص. 788-791، 4ص.

الناشر

المركز السعودي لزراعة الأعضاء

تاريخ النشر

2011-08-31

دولة النشر

السعودية

عدد الصفحات

4

التخصصات الرئيسية

الطب البشري

الموضوعات

الملخص EN

Jobber syndrome (JS) is a rare developmental disorder of the central nervous system, characterized by brainstem and cerebellar malformations, hypertonia, episodic hyper apnea and apnea and mental retardation.

It may be associated other systemic abnormalities like ocular (e.g., retinal dysplasia, etc.), coulometer, musculoskeletal and renal (e.g., cystic dysplasia, nephron phthisis), with renal failure.

We describe a case of JS with nephron phthisis in neurofibromatosis Type 1 leading to end-stage renal disease, an association that has never been described earlier in the medical literature to the best of our knowledge.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Ghamidi, Jawad Ahmad& Ali, Uma S.. 2011. Joubert syndrome with nephronophthisis in neurofibromatosis type 1. Saudi Journal of Kidney Diseases and Transplantation،Vol. 22, no. 4, pp.788-791.
https://search.emarefa.net/detail/BIM-268284

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Ghamidi, Jawad Ahmad& Ali, Uma S.. Joubert syndrome with nephronophthisis in neurofibromatosis type 1. Saudi Journal of Kidney Diseases and Transplantation Vol. 22, no. 4 (Aug. 2011), pp.788-791.
https://search.emarefa.net/detail/BIM-268284

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Ghamidi, Jawad Ahmad& Ali, Uma S.. Joubert syndrome with nephronophthisis in neurofibromatosis type 1. Saudi Journal of Kidney Diseases and Transplantation. 2011. Vol. 22, no. 4, pp.788-791.
https://search.emarefa.net/detail/BIM-268284

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 791

رقم السجل

BIM-268284