Cargando…
A novel syndrome of lethal familial hyperekplexia associated with brain malformation
BACKGROUND: Hyperekplexia (HPX) is a rare non-epileptic disorder manifesting immediately after birth with exaggerated persistent startle reaction to unexpected auditory, somatosensory and visual stimuli, and non-habituating generalized flexor spasm in response to tapping of the nasal bridge (glabell...
Autores principales: | Seidahmed, Mohammed Zein, Salih, Mustafa A, Abdulbasit, Omer B, Shaheed, Meeralebbae, Al Hussein, Khalid, Miqdad, Abeer M, Al Rasheed, Abdullah K, Alazami, Anas M, Alorainy, Ibrahim A, Alkuraya, Fowzan S |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488335/ https://www.ncbi.nlm.nih.gov/pubmed/23101555 http://dx.doi.org/10.1186/1471-2377-12-125 |
Ejemplares similares
-
Hyperekplexia, microcephaly and simplified gyral pattern caused by novel ASNS mutations, case report
por: Seidahmed, Mohammed Zain, et al.
Publicado: (2016) -
Genetic, chromosomal, and syndromic causes of neural tube defects
por: Seidahmed, Mohammed Z., et al.
Publicado: (2014) -
Epidemiology of neural tube defects
por: Seidahmed, Mohammed Z., et al.
Publicado: (2014) -
Novel IFT122 mutation associated with impaired ciliogenesis and cranioectodermal dysplasia
por: Alazami, Anas M, et al.
Publicado: (2014) -
TLE6 mutation causes the earliest known human embryonic lethality
por: Alazami, Anas M., et al.
Publicado: (2015)