Wolfram's (DIDMOAD)‎ syndrome and chronic renal failure

المؤلفون المشاركون

Hazza, Isa A.
Hassan, Mujalli Ahmad
Najad, Abd al-Hamid

المصدر

Saudi Journal of Kidney Diseases and Transplantation

العدد

المجلد 11، العدد 1 (28 فبراير/شباط 2000)، ص ص. 53-58، 6ص.

الناشر

المركز السعودي لزراعة الأعضاء

تاريخ النشر

2000-02-28

دولة النشر

السعودية

عدد الصفحات

6

التخصصات الرئيسية

الطب البشري

الموضوعات

الملخص EN

Wolfram’s syndrome is usually considered as an autosomal recessive condition, with wide phenotypic variation.

The syndrome is commonly called DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy and deafness), although some patients have additional clinical findings including ataxia, hypogonadism, hydronephrosis and psychiatric illnesses.

We report a patient with DIDMOAD syndrome with emphasis on the urological tract and its progressive complications.

Unfortunately, he developed end-stage renal failure and needed hemodialysis at the age of 14 years.

The presentation, investigations and management are discussed.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Hassan, Mujalli Ahmad& Najad, Abd al-Hamid& Hazza, Isa A.. 2000. Wolfram's (DIDMOAD) syndrome and chronic renal failure. Saudi Journal of Kidney Diseases and Transplantation،Vol. 11, no. 1, pp.53-58.
https://search.emarefa.net/detail/BIM-62141

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Hassan, Mujalli Ahmad…[et al.]. Wolfram's (DIDMOAD) syndrome and chronic renal failure. Saudi Journal of Kidney Diseases and Transplantation Vol. 11, no. 1 (Feb. 2000), pp.53-58.
https://search.emarefa.net/detail/BIM-62141

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Hassan, Mujalli Ahmad& Najad, Abd al-Hamid& Hazza, Isa A.. Wolfram's (DIDMOAD) syndrome and chronic renal failure. Saudi Journal of Kidney Diseases and Transplantation. 2000. Vol. 11, no. 1, pp.53-58.
https://search.emarefa.net/detail/BIM-62141

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 58

رقم السجل

BIM-62141