Syndrome in question

Costello syndrome (CS) is a rare genetic disorder, first described by Costello in 1971, caused by mutations in the HRAS proto-oncogene. Clinical findings include facial dysmorphism, skin disorders, cognitive impairment, cardiac and musculoskeletal defects. There is an increased risk of malignancies...

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Detalles Bibliográficos
Autores principales: Peixoto, Isy Lima, Carreno, Ana Maria, Prazeres, Vania Mesquita Gadelha, Chirano, Caroline Albuquerque Rodrigues, Ihara, Gabriel Maroja, Akel, Patricia Bandeira de Melo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2014
Materias:
Syndrome In Question
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230678/
https://www.ncbi.nlm.nih.gov/pubmed/25387514
http://dx.doi.org/10.1590/abd1806-4841.20143062

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230678/
https://www.ncbi.nlm.nih.gov/pubmed/25387514
http://dx.doi.org/10.1590/abd1806-4841.20143062

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