Nayab Munib, Iqbal Haider, Suleman Elahi.
Laurence-Moon-Bardet-Biedl Syndrome: a Case Report.
J Med Sci Jan ;30(03):227-9.

Laurence-Moon-Bardet-Biedl Syndrome (LMBBS) is a rare autosomal recessive innate disorder, ensuing as a result of consanguineous marriage. It characteristically manifests as a congenital ciliopathy with a saga of widely distinct primary and secondary clinical features. Patients with LMBBS experience rapid decline in the functionality of the brain, eyes, kidneys, hands, and feet. The cardinal features typical of the syndrome include mental retarda-tion, atypical retinitis pigmentosa, hypogonadism, poly-dactyly, obesity, and renal impairment.

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