Two Cases of Chromosome 22q11.2 Deletion Syndrome Diagnosed in 12-Year-Old Boys with Hypocalcemic Seizures

Chromosome 22q11.2 deletion syndrome is the most common interstitial deletion syndrome. Major clinical manifestation includes hypocalcemia secondary to hypoparathyroidim. At least 10% of the patients with this syndrome had hypocalcemic seizures which are generally improved over the first year of lif...

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Detalles Bibliográficos
Autores principales: Hyun, Jae Won, Chung, Hwa Kyoung, Kim, Sung-Hee, Choi, Ye Ji, Kim, Sung Jin, Kim, Hae Soon, Lee, Hyang Woon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Epilepsy Society 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952324/
https://www.ncbi.nlm.nih.gov/pubmed/24649462
http://dx.doi.org/10.14581/jer.12011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952324/
https://www.ncbi.nlm.nih.gov/pubmed/24649462
http://dx.doi.org/10.14581/jer.12011

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