Laurence-Moon-Bardet-Biedl syndrome
- PMID: 19079403
Laurence-Moon-Bardet-Biedl syndrome
Abstract
Laurence-Moon-Bardet-Biedl syndrome is a rare, genetically heterogeneous, autosomal recessive inherited disorder with wide variability in expression. We report a case of Laurence-Moon-Bardet-Biedl syndrome with typical phenotype in conjunction with nonalcoholic steatohepatitis. The diagnosis had been missed until the patient presented at our hospital.