Bardet–Biedl syndrome with nonalcoholic steatohepatitis, hypertension, and hypothyroidism
Bardet–Biedl syndrome (BBS) is a rare, genetically heterogeneous, autosomal recessive inherited disorder with wide variability in expression. The accepted major criteria for diagnosis include retinal dystrophy, obesity, polydactyly, male hypogonadism, mental retardation, and renal dysfunction. We ar...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2016-01-01
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Series: | CHRISMED Journal of Health and Research |
Subjects: | |
Online Access: | http://www.cjhr.org/article.asp?issn=2348-3334;year=2016;volume=3;issue=2;spage=128;epage=130;aulast=Singh |