Results 71 to 80 of about 1,298,739 (158)

Three cases of Wolfram syndrome with different clinical aspects.

, 2015
Wolfram syndrome is an autosomal recessive disorder caused by mutations in the WFS1 gene.
Çamtosun, E., Berberoğlu, M., Kocaay, P., Flanagan, Sarah, Ceylaner, S., Şıklar, Z., Ellard, Sian, ŞIKLAR, ZEYNEP, Kocaay, Pinar, Berberoʇlu, Merih, Flanagan, Sarah E., CEYLANER, SERDAR, Çamtosun, Emine   +12 more
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Microvascular Changes in Wolfram Syndrome

, 2020
Wolfram syndrome (WS) is a rare autosomal recessive progressive neurodegenerative disease. The purpose of this work is to evaluate systemic, genetic and ophthalmic characteristics, including optical coherence tomography angiography (OCTA) measurements of
Olinda Faria; Ana Maria Cunha; Sﾎrgio Estrela Silva; Fernando Falcﾋo-Reis
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Wolfram syndrome: A rare mimic of type 1 diabetes mellitus

CHRISMED Journal of Health and Research, 2016
Wolfram syndrome is a rare autosomal recessive disorder characterized by a constellation of disorders also known as diabetes insipidus, diabetes mellitus (DM), optic atrophy, and deafness.
Manish Gutch, Krishna Kumar Sahani, Annesh Bhattacharjee, Sukriti Kumar, Shobhit Shakya   +4 more
doaj   +1 more source

Thiamine– Responsive Megaloblastic Anemia Syndrome

Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, 2009
Thiamine Responsive megaloblastic anemia in DIDMOA (Wolfram) syndrome has an autosomal- recessive mode of inheritance . Megaloblastic anemia and sideroblastic anemia is accompanied by diabetes insipidus (DI), diabetes mellitus (DM) ,optic atrophy (OA ...
F Motavaselian, F Nourani, Kh Dehghani, M Kheirandish, AH Jafari, A Hashemi   +5 more
doaj  

Brief von Wolfram Mieth an Kurt Rothschild

BRIEF VON WOLFRAM MIETH AN KURT ROTHSCHILD Brief von Wolfram Mieth an Kurt Rothschild ([1]
Mieth, Wolfram
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Case report: hyponatraemia in Wolfram syndrome

Clinical Medicine
Introduction: The Wolfram or DIDMOAD (diabetes Insipidus, diabetes mellitus, optic atrophy, and deafness) syndrome is characterised by arginine-vasopressin deficiency, diabetes mellitus, optic atrophy and deafness, with cognitive and psychiatric issues ...
Khadijah Tukur, Zakari Sani
doaj   +1 more source

Wolfram to Alstrom: Analysis of a Diagnostic Error

Online Journal of Health & Allied Sciences, 2021
Wolfram syndrome (DIDMOAD) and Alstrom syndrome are two rare, clinically similar diseases inherited in an autosomal recessive pattern. We report the case of a 19 year old male who presented with left upper abdominal mass and two episodes of high coloured
Annapoorna Chakrabarty, Shipra Rai, Kavitha Saravu   +2 more
doaj  

Wolfram syndrome by the means of three patients

, 2007
Wolfram sendromu diabetes insipidus. diabetes mellitus. optik atrofi ve işitme kaybının eşlik ettiği nörodejeneratif hastalıktır. Bir aileden 3 olgu nedeniyle Wolfram sendromunun oftalmolojik ve sistemik bulguları rapor edilmiştir.Content : Wolfram ...
Ali Fuat Şaşoğlu, Melis Palamar, Süheyla Köse, Tahir Atik, Önder Üretmen   +4 more
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Exenatide Is an Effective Antihyperglycaemic Agent in a Mouse Model of Wolfram Syndrome 1

Journal of Diabetes Research, 2016
Wolfram syndrome 1 is a very rare monogenic disease resulting in a complex of disorders including diabetes mellitus. Up to now, insulin has been used to treat these patients. Some of the monogenic forms of diabetes respond preferentially to sulphonylurea
Tuuli Sedman, Kertu Rünkorg, Maarja Krass, Hendrik Luuk, Mario Plaas, Eero Vasar, Vallo Volke   +6 more
doaj   +1 more source

Various clinical aspects of DIDMOAD (Wolfram) syndrome

, 1995
The association of juvenile diabetes mellitus (DM), diabetes insipidus (DI), optic atrophy (OA) and sensorineural deafness (D) is known as DIDMOAD or Wolfram syndrome.
OKTEN, AYŞE NUR, MOCAN, H, DEMIRCI, ALİ, Erduran, EROL, GEDIK, YUSUF, ASLAN, YAKUP   +5 more
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