Source:http://linkedlifedata.com/resource/pubmed/id/16669965
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2006-5-3
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pubmed:abstractText |
Alstrom syndrome is a rare autosomal recessive disorder characterized by retinal degeneration, sensorineural hearing loss, obesity, type 2 diabetes mellitus and chronic nephropathy. It may be associated with acanthosis nigricans, hypergonadotropic hypogonadism, hepatic dysfunction, hepatic steatosis, hyperlipidaemia, dilated cardiomyopathy and short stature. We report a patient with Alstrom syndrome who had hypergonadotropic hypogonadism, hepatic dysfunction, hepatic steatosis and short stature with normal body weight, all of which are seen infrequently with this syndrome.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1320-5358
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
81-4
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pubmed:meshHeading |
pubmed-meshheading:16669965-Adult,
pubmed-meshheading:16669965-Blood Glucose,
pubmed-meshheading:16669965-Body Height,
pubmed-meshheading:16669965-Creatinine,
pubmed-meshheading:16669965-Diabetes Mellitus,
pubmed-meshheading:16669965-Diagnosis, Differential,
pubmed-meshheading:16669965-Fatty Liver,
pubmed-meshheading:16669965-Growth Disorders,
pubmed-meshheading:16669965-Humans,
pubmed-meshheading:16669965-Hypogonadism,
pubmed-meshheading:16669965-Kidney Diseases,
pubmed-meshheading:16669965-Male,
pubmed-meshheading:16669965-Retinitis Pigmentosa,
pubmed-meshheading:16669965-Syndrome
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pubmed:year |
2006
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pubmed:articleTitle |
Rare case of Alstrom syndrome without obesity and with short stature, diagnosed in adulthood.
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pubmed:affiliation |
Department of Internal Medicine, Atatürk Teaching and Research Hospital, Ankara, Turkey. koceyup@yahoo.com
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pubmed:publicationType |
Journal Article,
Case Reports
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