Laurence-Moon-Bardet-Biedl Syndrome: A Case Report

Laurence-Moon-Bardet-Biedl syndrome (LMBBS), a rare autosomal recessive defect, mostly occurs in children born from consanguineous marriages. The major features of this syndrome are cone-rod dystrophy, polydactyly, obesity, learning disabilities, hypogonadism in males, renal anomalies, nystagmus, sp...

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Detalles Bibliográficos
Autores principales: Khan, Bilal Ahmed, Shahid, Ashar, Bin Nazir, Maaz, Khan, Kiran Shafiq, Punshi, Avinash
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2019
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820889/
https://www.ncbi.nlm.nih.gov/pubmed/31696011
http://dx.doi.org/10.7759/cureus.5618

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820889/
https://www.ncbi.nlm.nih.gov/pubmed/31696011
http://dx.doi.org/10.7759/cureus.5618

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