Saudi Journal of Kidney Diseases and Transplantation

CASE REPORT
Year
: 2000  |  Volume : 11  |  Issue : 1  |  Page : 53--58

Wolfram«SQ»s (DIDMOAD) Syndrome and Chronic Renal Failure


Mojaly Ahmed Hasan, Issa Hazza, Abdulhamid Najada 
 Pediatric Unit, King Hussein Medical Center, Amman, Jordan

Correspondence Address:
Mojaly Ahmed Hasan
Pediatric Consultant, King Hussein Medical Center, P.O. Box 6080, El-Zarqa
Jordan

Wolfram«SQ»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.


How to cite this article:
Hasan MA, Hazza I, Najada A. Wolfram's (DIDMOAD) Syndrome and Chronic Renal Failure.Saudi J Kidney Dis Transpl 2000;11:53-58


How to cite this URL:
Hasan MA, Hazza I, Najada A. Wolfram's (DIDMOAD) Syndrome and Chronic Renal Failure. Saudi J Kidney Dis Transpl [serial online] 2000 [cited 2021 Jul 24 ];11:53-58
Available from: https://www.sjkdt.org/article.asp?issn=1319-2442;year=2000;volume=11;issue=1;spage=53;epage=58;aulast=Hasan;type=0