Bardet-Biedl syndrome

*Gene map locus 20p12, 16q21, 15q22.3-q23, 14q32.1, 11q13, 4q27, 3p12-q13, 2q31

BBS

Laurence-Moon-Bardet-Biedl syndrome

[Clinical features: rod-cone dystrophy; postaxial polydactyly; central obesity; mental retardation; hypogonadism; renal dysfunction]

[Inheritance: autosomal recessive]

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Intrafamilial variation of the phenotype in Bardet-Biedl syndrome	Intrafamilial variation of the phenotype in Bardet-Biedl syndrome	Intrafamilial variation of the phenotype in Bardet-Biedl syndrome
British Journal of Ophthalmology	British Journal of Ophthalmology	British Journal of Ophthalmology


Bardet-Biedl syndrome: A case report	Bardet-Biedl syndrome: A case report	Exploring the molecular basis of Bardet-Biedl syndrome
Dermatology Online Journal	Dermatology Online Journal	Human Molecular Genetics


A Case of Bardet Biedl Syndrome	A Case of Bardet Biedl Syndrome	A Case of Bardet Biedl Syndrome
Internet Journal of Pediatrics and Neonatology	Internet Journal of Pediatrics and Neonatology	Internet Journal of Pediatrics and Neonatology


Does Bardet-Biedl syndrome have a characteristic face?	New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey	New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey
Journal of Medical Genetics	Journal of Medical Genetics	Journal of Medical Genetics


Bardet-Biedl Syndrome with Rheumatic Aortic Regurgitation	Bardet-Biedl Syndrome with Rheumatic Aortic Regurgitation	An infant with polydactyly and renal anomalies: early diagnosis of a rare syndrome
Journal of The Association of Physicians of India	Journal of The Association of Physicians of India	Nephrology Dialysis Transplantation

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