نتایج جستجو برای: didmoad .

تعداد نتایج: 60  

Journal: :Diabetes care 2007
Aline Cano Laurent Molines René Valéro Gilbert Simonin Véronique Paquis-Flucklinger Bernard Vialettes

OBJECTIVE Some previous studies suggested that patients suffering from Wolfram syndrome or DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness) might be relatively preserved from diabetic retinopathy and nephropathy. However, these data were not conclusive because either observations were only anecdotic or did not match with control type 1 diabetic populations. RESEARC...

Journal: :Archives of Disease in Childhood 1978

Journal: :British Journal of Psychiatry 1994

Journal: :Journal of Medical Genetics 1997

Journal: :Journal of medical genetics 1994
D Pilz O W Quarrell E W Jones

DIDMOAD is usually considered an autosomal recessive condition, with wide phenotypic variation, but the possibility of mitochondrial mutations occurring in this condition has been considered. A 19 year old man presented with long standing diabetes mellitus, optic atrophy, and grand mal seizures. Further investigations showed unilateral sensorineural hearing loss and the most common mitochondria...

Journal: :Journal of Clinical and Analytical Medicine 2013

Journal: :Postgraduate Medical Journal 1986

Journal: :Archives of disease in childhood 1995
A T Soliman B Bappal A Darwish A Rajab M Asfour

Two girls with DIDMOAD syndrome are presented. One also had severe megaloblastic-sideroblastic anaemia and the other several neurological manifestations. Both were short with defective growth hormone secretion. Computed tomography revealed empty sella in both girls; one had widespread atrophic cortical and cerebellar changes. High doses of thiamine improved the anaemia in the first case, increa...

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