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DIDMOAD Syndrome (Wolfram Syndrome) in Four Male Siblings
Pediatrics International, 1987AbstractFour male siblings including two typical cases of DIDMOAD syndrome are described. The typical cases were aged 16 and 15, with diabetes insipidus, insulin‐dependent diabetes mellitus (IDDM), optic atrophy, perceptive hearing loss, dilatation of the urinary tract and disturbed EEC One of the others was aged 10, with bilateral concentric ...
S, Kumaki, H, Mori, H, Suzuki
exaly +3 more sources
Cranial magnetic resonance imaging of Wolfram (DIDMOAD) syndrome
Journal of Medical Imaging and Radiation Oncology, 2005 Wolfram syndrome is a rare neurodegenerative disorder characterized by diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD). A wide spectrum of abnormalities of the central nervous system, urinary tract and endocrine glands is also
Emre Pakdemirli
exaly +2 more sources
DIDMOAD syndrome in a Libyan family
Annals of Tropical Paediatrics, 1986We report three Libyan children from one family with the syndrome diabetes insipidus, diabetes mellitus, optic atrophy and deafness, (DIDMOAD). Two children presented with diabetic ketoacidosis while one was discovered during screening of the family. All three children are alive, two of them on desmopressin (DDAVP) and insulin therapy and one on DDAVP ...
N M, Shembesh +3 more
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Thiamine-responsive anemia in DIDMOAD syndrome
The Journal of Pediatrics, 1989Two children with the DIDMOAD syndrome (diabetes insipidus, diabetes mellitus, optic atrophy, deafness) developed a megaloblastic and sideroblastic anemia, neutropenia, and borderline thrombocytopenia. Plasma thiamine concentration was low in one patient and normal in the other; in both children, thiamine pyrophosphate in erythrocytes and thiamine ...
C, Borgna-Pignatti +4 more
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Wiener medizinische Wochenschrift (1946), 1994
The DIDMOAD or so called Wolfram syndrome is a hereditary disease with autosomal-recessive transmission showing 4 main features: diabetes mellitus, diabetes insipidus, nervus opticus atrophia and deafness. Beside this it shows multiple organ involvement.
R, Alicanoğlu +6 more
openaire +1 more source
The DIDMOAD or so called Wolfram syndrome is a hereditary disease with autosomal-recessive transmission showing 4 main features: diabetes mellitus, diabetes insipidus, nervus opticus atrophia and deafness. Beside this it shows multiple organ involvement.
R, Alicanoğlu +6 more
openaire +1 more source