Acute Dystonia in a Patient with 22q11.2 Deletion Syndrome

The 22q11.2 deletion syndrome (di George syndrome) is one of the most prevalent genetic disorders. The clinical features of the syndrome are distinct facial appearance, velopharyngeal insufficiency, conotruncal heart disease, parathyroid and immune dysfunction; however, little is known about possibl...

Descripción completa

Detalles Bibliográficos
Autores principales: Kontoangelos, Konstantinos, Maillis, Antonis, Maltezou, Maria, Tsiori, Sofia, Papageorgiou, Charalambos C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620283/
https://www.ncbi.nlm.nih.gov/pubmed/26605035
http://dx.doi.org/10.4081/mi.2015.5902

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620283/
https://www.ncbi.nlm.nih.gov/pubmed/26605035
http://dx.doi.org/10.4081/mi.2015.5902

Ejemplares similares