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Volumn 2, Issue 1, 2009, Pages 98-103
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Rare case of Alstrom syndrome with empty sella and interfamilial presence of Bardet-Biedl phenotype.
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Author keywords
[No Author keywords available]
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Indexed keywords
HUMAN GROWTH HORMONE;
ADULT;
ALSTROM SYNDROME;
ARTICLE;
BARDET BIEDL SYNDROME;
BLINDNESS;
CASE REPORT;
CONGESTIVE CARDIOMYOPATHY;
EMPTY SELLA SYNDROME;
EUKARYOTIC FLAGELLUM;
GENETICS;
HUMAN;
HYPERTENSION;
MALE;
NON INSULIN DEPENDENT DIABETES MELLITUS;
OBESITY;
PEDIGREE;
PERCEPTION DEAFNESS;
PHENOTYPE;
PHYSIOLOGY;
ALSTROM SYNDROME;
BARDET-BIEDL SYNDROME;
BLINDNESS;
CARDIOMYOPATHY, DILATED;
CILIA;
DIABETES MELLITUS, TYPE 2;
EMPTY SELLA SYNDROME;
HEARING LOSS, SENSORINEURAL;
HUMAN GROWTH HORMONE;
HUMANS;
HYPERTENSION;
MALE;
OBESITY;
PEDIGREE;
PHENOTYPE;
YOUNG ADULT;
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EID: 77649200625
PISSN: 1844122X
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (6)
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References (0)
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