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  • Title: Laurence-Moon-Bardet-Biedl syndrome.
    Author: Sahu JK, Jain V.
    Journal: JNMA J Nepal Med Assoc; 2008; 47(172):235-7. PubMed ID: 19079403.
    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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