An Eight Month Old Male Child with Laurence-Moon-Bardet-Biedl Syndrome: A Case Report
Journal Title: Scholars Journal of Medical Case Reports - Year 2015, Vol 3, Issue 4
Abstract
Abstract: Laurence-Moon-Bardet-Biedl syndrome (LMBBS) is an important entity among the paediatric syndromes. It is an autosomal recessively transmitted genetic disorder. LMBBS is characterized by obesity, retinal degeneration, extra digits on the hands and feet (polydactyly), intellectual impairment and hypogonadism. The syndrome has historic importance as initially it was known as the LMBBS and then it is recently subcategorised into the well famous Laurence-Moon Syndrome (LMS) and the well published Bardet-Biedl Syndrome (BBS). We present a case report of a eight month old male child with LMBBS. Keywords: Laurence-Moon-Bardet-Biedl Syndrome (LMBBS), Obesity, Polydactyly, Mental retardation, Hypogonadism.
Authors and Affiliations
Menon Narayanankutty Sunilkumar, Vadakut Krishnan Parvathy
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