Laurence-Moon-Bardet-Biedl Syndrome: A case report

Laurence-Moon-Bardet-Biedl Syndrome: A case report

Laurence-Moon-Bardet-Beidl syndrome is a rare ciliopathic and pleiotropic human autosomal recessive genetic disorder.1 In 1886, Laurence and Moon explained a case of a 7-year-old female with rod-cone dystrophy, hypogenitalism, mental retardation, obesity, and polydactyly. In 1920, Bardet described a...

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Bibliographic Details
Main Authors:	Md. Mozammel Haque, Kamrunnaher Shultana, Tahmina Binte Matin, Md. Shohidul Islam Khan, Abdullah Al Baki
Format:	Article
Language:	English
Published:	Indonesian Pediatric Society Publishing House 2019-11-01
Series:	Paediatrica Indonesiana
Subjects:	obesity; retinitis pigmentosa; polydactyly; mental retardationpigmentosa
Online Access:	https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/2097

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