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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APA
Sahu, J. K., & Jain, V. (2008). Laurence-Moon-Bardet-Biedl syndrome. Journal of the Nepal Medical Association, 47(172), 235–237. https://doi.org/10.31729/jnma.166
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