Literature DB >> 15526727

Wolfram (DIDMOAD) syndrome: report of two patients.

Chao-Hsu Lin1, Yann-Jinn Lee, Chi-Yu Huang, Jui-Wen Shieh, Hung-Ching Lin, An-Mei Wang, Bing-Fu Shih.   

Abstract

We report a girl with Wolfram syndrome who presented with juvenile-onset diabetes mellitus when she was 4 3/12 years old. Optic atrophy and high frequency sensorineural hearing loss were found at 7 and 9 5/12 years of age, respectively. Her younger brother also developed Wolfram syndrome when he was 3 2/12 years old. Wolfram syndrome is also called DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy and deafness). This syndrome is transmitted as an autosomal recessive trait and is a progressive neurodegenerative disorder. It should be considered in a diabetic patient with unexplained optic atrophy, hearing loss, or polyuria and polydipsia in the presence of adequate blood glucose control. Visual acuity should be checked annually in patients with juvenile-onset diabetes mellitus. Optic atrophy should be considered if visual acuity is impaired.

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Year:  2004        PMID: 15526727     DOI: 10.1515/jpem.2004.17.10.1461

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  2 in total

1.  The value of urine specific gravity in detecting diabetes insipidus in a patient with uncontrolled diabetes mellitus: urine specific gravity in differential diagnosis.

Authors:  Ersin Akarsu; Hakan Buyukhatipoglu; Sebnem Aktaran; Ramazan Geyik
Journal:  J Gen Intern Med       Date:  2006-11       Impact factor: 5.128

2.  Epidemiology and phenotypes of diabetes in children and adolescents in non-European-origin populations in or from Western Pacific region.

Authors:  Steven James; Jayanthi Maniam; Pik-To Cheung; Tatsuhiko Urakami; Julia von Oettingen; Supawadee Likitmaskul; Graham Ogle
Journal:  World J Clin Pediatr       Date:  2022-03-09
  2 in total

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