Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for “double trouble” overlapping syndromes

BACKGROUND: We report on a patient with genetically confirmed overlapping diagnoses of CMT1A and FSHD. This case adds to the increasing number of unique patients presenting with atypical phenotypes, particularly in FSHD. Even if a mutation in one disease gene has been found, further genetic testing...

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Detalles Bibliográficos
Autores principales: Schreiber, Olivia, Schneiderat, Peter, Kress, Wolfram, Rautenstrauss, Bernd, Senderek, Jan, Schoser, Benedikt, Walter, Maggie C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848428/
https://www.ncbi.nlm.nih.gov/pubmed/24041033
http://dx.doi.org/10.1186/1471-2350-14-92

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848428/
https://www.ncbi.nlm.nih.gov/pubmed/24041033
http://dx.doi.org/10.1186/1471-2350-14-92

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