Rare case of Alstrom syndrome with empty sella and interfamilial presence of Bardet-Biedl phenotype. [electronic resource]
Producer: 20100305Description: 98-103 p. digitalISSN:- 1844-122X
- Alstrom Syndrome -- genetics
- Bardet-Biedl Syndrome -- genetics
- Blindness -- genetics
- Cardiomyopathy, Dilated -- genetics
- Cilia -- physiology
- Diabetes Mellitus, Type 2 -- genetics
- Empty Sella Syndrome -- genetics
- Hearing Loss, Sensorineural -- genetics
- Human Growth Hormone -- deficiency
- Humans
- Hypertension -- genetics
- Male
- Obesity -- genetics
- Pedigree
- Phenotype
- Young Adult
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Publication Type: Case Reports; Journal Article
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