Wolfram syndrome

Wolfram syndrome [26] A syndrome of DIDMOAD. While most cases have been ascribed to an autosomal recessive gene mapping to chromosome 4pl6, some cases of early-onset DIDMOAD might result from mtDNA mutations or deletions. 

Liu, X.R., Vansant, G., Udovichenko, I.P, Wolfram, U. and Williams, D.S. (1997) Myosin Vila, the product of the Usher IB syndrome gene, is concentrated in the connecting cilia of photoreceptor cells. Cell Motil. Cytoskeleton 37, 240-252. 

Other genetic syndromes sometimes associated with diabetes Down s syndrome Klinefelter s syndrome Turner s syndrome Wolfram s syndrome Friedreich s ataxia Huntington s chorea Laurence-Moon-Bieldel syndrome Myotonic dystrophy Porphyria... 

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