Seizures as the first manifestation of chromosome 22q11.2 deletion syndrome in a 40-year old man: a case report

BACKGROUND: The microdeletion of chromosome 22q11.2 is the most common human deletion syndrome. It typically presents early in life and is rarely considered in adult patients. As part of the manifestations of this condition, patients can have parathyroid glandular involvement ranging from hypocalcem...

Descripción completa

Detalles Bibliográficos
Autores principales: Tonelli, Adriano R, Kosuri, Kalyan, Wei, Sainan, Chick, Davoren
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222674/
https://www.ncbi.nlm.nih.gov/pubmed/18053182
http://dx.doi.org/10.1186/1752-1947-1-167

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222674/
https://www.ncbi.nlm.nih.gov/pubmed/18053182
http://dx.doi.org/10.1186/1752-1947-1-167

Ejemplares similares