Four-year follow-up study in a NF1 Boy with a focal pontine hamartoma

Neurofibromatosis is a collective name for a group of genetic conditions in which benign tumours affect the nervous system. Type 1 is caused by a genetic mutation in the NF1 gene (OMIM 613113) and symptoms can vary dramatically between individuals, even within the same family. Some people have very...

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Detalles Bibliográficos
Autores principales: Parisi, Pasquale, Persechino, Severino, Paolino, Maria Chiara, Nicita, Francesco, Torrente, Isabella, Bozzao, Alessandro, Villa, Maria Pia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3579694/
https://www.ncbi.nlm.nih.gov/pubmed/23399325
http://dx.doi.org/10.1186/1824-7288-39-10

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3579694/
https://www.ncbi.nlm.nih.gov/pubmed/23399325
http://dx.doi.org/10.1186/1824-7288-39-10

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