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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2007-1-1
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pubmed:abstractText |
Wolfram syndrome (WS) is an autosomal recessive disorder characterized by the association of juvenile-onset diabetes mellitus and optic atrophy. It is also known by the acronym DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness).
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0172-780X
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
27
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
691-4
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pubmed:meshHeading |
pubmed-meshheading:17187023-Age of Onset,
pubmed-meshheading:17187023-Gene Deletion,
pubmed-meshheading:17187023-Humans,
pubmed-meshheading:17187023-Male,
pubmed-meshheading:17187023-Membrane Proteins,
pubmed-meshheading:17187023-Mental Disorders,
pubmed-meshheading:17187023-Pedigree,
pubmed-meshheading:17187023-Severity of Illness Index,
pubmed-meshheading:17187023-Suicide,
pubmed-meshheading:17187023-Urologic Diseases,
pubmed-meshheading:17187023-Wolfram Syndrome
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pubmed:year |
2006
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|
pubmed:articleTitle |
A new mutation in WFS1 gene (C.1522-1523delTA, Y508fsX421) may be responsible for early appearance of clinical features of Wolfram syndrome and suicidal behaviour.
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pubmed:affiliation |
Department of Neurology, School of Medicine, Dicle University, Diyarbakir, Turkey. aluclu@dicle.edu.tr
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pubmed:publicationType |
Journal Article,
Case Reports
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