نتایج جستجو برای: wolfram syndrome

تعداد نتایج: 623455  

2017
Cécile Rouzier David Moore Cécile Delorme Sandra Lacas-Gervais Samira Ait-El-Mkadem Konstantina Fragaki Florence Burté Valérie Serre Sylvie Bannwarth Annabelle Chaussenot Martin Catala Patrick Yu-Wai-Man Véronique Paquis-Flucklinger

Wolfram syndrome (WS) is a progressive neurodegenerative disease characterized by early-onset optic atrophy and diabetes mellitus, which can be associated with more extensive central nervous system and endocrine complications. The majority of patients harbour pathogenic WFS1 mutations, but recessive mutations in a second gene, CISD2, have been described in a small number of families with Wolfra...

2014
Stefano Ghirardello Elisa Dusi Bianca Castiglione Monica Fumagalli Fabio Mosca

BACKGROUND Wolfram syndrome (WS) is an autosomal recessive neurodegenerative disorder characterized by diabetes mellitus (DM), optic atrophy (OA), central diabetes insipidus (CDI) and deafness (D). The phenotype of the disease has been associated with several mutations in the WFS1 gene, a nuclear gene localized on chromosome 4. Since the discovery of the association between WFS1 gene and Wolfra...

Journal: :Indian Journal of Clinical Biochemistry 2009

2016
Tuuli Sedman Kertu Rünkorg Maarja Krass Hendrik Luuk Mario Plaas Eero Vasar Vallo Volke

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 preparations. The aim of the current study was to elucidate whether exenatide, a GLP-1 receptor agonist, and glipizide, a sulphonylurea, are e...

2017
Dewi Astuti Ataf Sabir Piers Fulton Malgorzata Zatyka Denise Williams Carol Hardy Gabriella Milan Francesca Favaretto Patrick Yu-Wai-Man Julia Rohayem Miguel López de Heredia Tamara Hershey Lisbeth Tranebjaerg Jian-Hua Chen Annabel Chaussenot Virginia Nunes Bess Marshall Susan McAfferty Vallo Tillmann Pietro Maffei Veronique Paquis-Flucklinger Tarekign Geberhiwot Wojciech Mlynarski Kay Parkinson Virginie Picard Gema Esteban Bueno Renuka Dias Amy Arnold Caitlin Richens Richard Paisey Fumihiko Urano Robert Semple Richard Sinnott Timothy G Barrett

We developed a variant database for diabetes syndrome genes, using the Leiden Open Variation Database platform, containing observed phenotypes matched to the genetic variations. We populated it with 628 published disease-associated variants (December 2016) for: WFS1 (n = 309), CISD2 (n = 3), ALMS1 (n = 268), and SLC19A2 (n = 48) for Wolfram type 1, Wolfram type 2, Alström, and Thiamine-responsi...

 Wolfram Syndrome is a neurodegenerative autosomal recessive disorder. The occurrence of the disease should be suspected if non-autoimmune insulin-dependent diabetes occurs in an under-sixteen year old person having bilateral optic nerve atrophy. Diabetes insipidus (DI), neurosensory deafness, urinary track disorders, and nervous system complications are also seen in this disorder. The current ...

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