Laurence-Moon-Bardet-Biedl Syndrome: A Rare Case With a Literature Review

Laurence-Moon-Bardet-Biedl syndrome (LMBBS), a rare autosomal recessive genetic disorder, results from consanguineous marriage. It is a congenital ciliopathy manifesting with primary and secondary characteristics. Primary clinical features include rod and cone dystrophy, polydactyly, central obesity...

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Detalles Bibliográficos
Autores principales: Kumar, Aneel, Husain, Aamir, Saleem, Amna, Khawaja, Uzzam Ahmed, Virani, Sumaira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720918/
https://www.ncbi.nlm.nih.gov/pubmed/33304690
http://dx.doi.org/10.7759/cureus.11355

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720918/
https://www.ncbi.nlm.nih.gov/pubmed/33304690
http://dx.doi.org/10.7759/cureus.11355

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