Catrinoiu, D <br/><br/>
Rare case of Alstrom syndrome with empty sella and interfamilial presence of Bardet-Biedl phenotype.  [electronic resource] 

 -  Journal of medicine and life   
 - 98-103 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1844-122X 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alstrom Syndrome--genetics<br/>Bardet-Biedl Syndrome--genetics<br/>Blindness--genetics<br/>Cardiomyopathy, Dilated--genetics<br/>Cilia--physiology<br/>Diabetes Mellitus, Type 2--genetics<br/>Empty Sella Syndrome--genetics<br/>Hearing Loss, Sensorineural--genetics<br/>Human Growth Hormone--deficiency<br/>Humans<br/>Hypertension--genetics<br/>Male<br/>Obesity--genetics<br/>Pedigree<br/>Phenotype<br/>Young Adult