Neurofibromatosis Type 1 Complicated by Atypical Coarctation of the Thoracic Aorta

Neurofibromatosis type 1 (NF1) is a relatively common autosomal dominant genetic disorder with a prevalence of 1 in 3,000 (0.03%) at birth. Clinical features are café-au-lait macules, intertriginous freckling, dermal neurofibroma, iris hamartoma (Lisch nodules), and learning disability. NF1 vasculop...

Descripción completa

Detalles Bibliográficos
Autores principales: Kimura, Masato, Kakizaki, Shuhei, Kawano, Kengo, Sato, Shinichi, Kure, Shigeo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3603612/
https://www.ncbi.nlm.nih.gov/pubmed/23533898
http://dx.doi.org/10.1155/2013/458543

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3603612/
https://www.ncbi.nlm.nih.gov/pubmed/23533898
http://dx.doi.org/10.1155/2013/458543

Ejemplares similares