Literature DB >> 18209300

Wolfram's (DIDMOAD) Syndrome and Chronic Renal Failure.

M A Hasan1, I Hazza, A Najada.   

Abstract

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.

Entities:  

Year:  2000        PMID: 18209300

Source DB:  PubMed          Journal:  Saudi J Kidney Dis Transpl        ISSN: 1319-2442


  3 in total

Review 1.  Wolfram syndrome, a rare neurodegenerative disease: from pathogenesis to future treatment perspectives.

Authors:  Maria Teresa Pallotta; Giorgia Tascini; Roberta Crispoldi; Ciriana Orabona; Giada Mondanelli; Ursula Grohmann; Susanna Esposito
Journal:  J Transl Med       Date:  2019-07-23       Impact factor: 5.531

Review 2.  Urinary Tract Involvement in Wolfram Syndrome: A Narrative Review.

Authors:  Alberto La Valle; Gianluca Piccolo; Mohamad Maghnie; Giuseppe d'Annunzio
Journal:  Int J Environ Res Public Health       Date:  2021-11-15       Impact factor: 3.390

3.  A case of Wolfram syndrome with chronic renal failure.

Authors:  Hüseyin Anıl Korkmaz
Journal:  Ann Pediatr Endocrinol Metab       Date:  2018-09-28
  3 in total

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