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Case Reports
. 2008 Oct-Dec;47(172):235-7.

Laurence-Moon-Bardet-Biedl syndrome

Affiliations
  • PMID: 19079403
Case Reports

Laurence-Moon-Bardet-Biedl syndrome

J K Sahu et al. JNMA J Nepal Med Assoc. 2008 Oct-Dec.

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.

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