Results 141 to 150 of about 1,384 (167)

Vasopressin Secretion in the DIDMOAD (Wolfram) Syndrome

QJM: An International Journal of Medicine, 1989
Abstract SUMMARY The diabetes insipidus which accompanies the DIDMOAD (Wolfram) Syndrome is thought to be hypothalamic in origin, though no formal study of vasopressin secretion in the syndrome has been published, and some data in the literature suggest arenal tubular defect.
C J, Thompson, J, Charlton, S, Walford, J, Baird, J, Hearnshaw, A, McCulloch, W, Kelly, P H, Baylis   +7 more
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DIDMOAD (Wolfram) syndrome [Letter]

, 1994
Kellner, M., Strian, F., Fassbender, K., Kennerknecht, I., Klein, R.   +4 more
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Three Cases of Didmoad or Wolfram’s Syndrome: Urological Aspects

Journal of Urology, 1992
We report on 3 patients with the rare syndrome of diabetes insipidus, diabetes mellitus, optic atrophy, neurosensory deafness, atony of the urinary tract and other abnormalities (DIDMOAD or Wolfram's syndrome). All 3 patients had diabetes mellitus, optic atrophy, deafness and dilatation of the urinary tract.
A, Thanos, A, Farmakis, Z, Sami, E, Davillas, N, Davillas   +4 more
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[Wolfram syndrome or DIDMOAD syndrome].

Archives francaises de pediatrie, 1984
The authors report a case of Wolfram's syndrome and discuss the evolution of the symptoms in relation with the data in the literature. The possibility of an association of Wolfram's syndrome with the HLA system is suggested. The use of carbamazepine in the treatment of the diabetes insipidus present in this syndrome is discussed.
A, Sarría, A, Legido, J M, Garagorri, T, Palomar, I, González, M, Bueno   +5 more
openaire   +1 more source

Neurodegeneration and Diabetes: Nationwide Study of Wolfram (DIDMOAD) Syndrome

Clinical Science, 1995
Wolfram syndrome is the association of diabetes mellitus and optic atrophy, and is sometimes called DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness). Incomplete characterisation of this autosomal recessive syndrome has relied on case-reports, and there is confusion with mitochondrial genome disorders.
T G, Barrett, S E, Bundey, A F, Macleod
openaire   +2 more sources

Wolfram (DIDMOAD) Syndrome: Case Report

2021
ÖzetWolfram sendromu, diyabetes mellitus, optik atrofi, diyabetes insipitus, işitme kaybı ile karakterize otozomal resesif geçiş gösteren genetik bir hastalıktır. Hastalarda nörolojik rahatsızlıklar, üriner sistem hastalıkları ve psikolojik rahatsızlıklarda izlenir.
ALTUN, Eda, PAYDAS, Saime, KAYA, Bülent, KARAYAYLALI, İbrahim   +3 more
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Otologic findings of DIDMOAD syndrome.

The American journal of otology, 1991
Two brothers with DIDMOAD (Wolfram) syndrome are described. The elder brother is 12 years old and was diagnosed as having diabetes mellitus at five. He later developed optic atrophy. The younger brother is 10 years old. He also has suffered from diabetes mellitus and optic atrophy. Their audiograms showed moderate hearing loss only at 8000 Hz. Auditory
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Mitochondrial diabetes, DIDMOAD and other inherited diabetes syndromes

Best Practice & Research Clinical Endocrinology & Metabolism, 2001
Inherited diabetes syndromes are individually rare but collectively make up a significant proportion of patients attending diabetes clinics, some of whom have multiple handicaps. This chapter focuses on syndromes in which major advances have been made in our understanding of the underlying molecular genetics.
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Wolfram syndrome: DIDMOAD

The British Journal of Diabetes & Vascular Disease, 2005
Deborah J Wake, Vittal Jadhav, Laurie R Whittome, Ian W Campbell   +3 more
openaire   +1 more source

DIDMOAD Syndrome and HLA-DR Haplotypes

Hormone and Metabolic Research, 1989
T W, van Haeften, P P, Razenberg
openaire   +2 more sources