Hyperekplexia, microcephaly and simplified gyral pattern caused by novel ASNS mutations, case report

BACKGROUND: Asparagine synthetase deficiency (OMIM# 615574) is a very rare newly described neurometabolic disorder characterized by congenital microcephaly and severe global developmental delay, associated with intractable seizures or hyperekplexia. Brain MRI typically shows cerebral atrophy with si...

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Detalles Bibliográficos
Autores principales: Seidahmed, Mohammed Zain, Salih, Mustafa A., Abdulbasit, Omer B., Samadi, Abdulmohsen, Al Hussien, Khalid, Miqdad, Abeer M., Biary, Maha S., Alazami, Anas M., Alorainy, Ibrahim A., Kabiraj, Mohammad M., Shaheen, Ranad, Alkuraya, Fowzan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947274/
https://www.ncbi.nlm.nih.gov/pubmed/27422383
http://dx.doi.org/10.1186/s12883-016-0633-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947274/
https://www.ncbi.nlm.nih.gov/pubmed/27422383
http://dx.doi.org/10.1186/s12883-016-0633-0

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