Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Rayan Magsi"'
Publikováno v:
Translation, Vol 11, Iss 2 (2023)
Introduction: Doose Syndrome is a myoclonic-atonic seizure disorder most prominent in the pediatric population. Several common genetic mutations have been identified. However, SUOX gene mutations have not yet been correlated with Doose Syndrome.
Externí odkaz:
https://doaj.org/article/97e9db4b12484079a7b2264d058ec5f2
Autor:
Payam Sadry, Rayan Magsi, Maahum Ahmed, Jennifer Amsdell, Talal Derani, Naeem Mahfooz, Ajaz Sheikh
Publikováno v:
Translation, Vol 11, Iss 2 (2023)
Introduction: Behçet’s disease (BD) is a rare inflammatory autoimmune disorder characterized by recurrent oral and genital ulcers, uveitis, and other systemic manifestations. Reported neurological manifestations of BD include meningoencephaliti
Externí odkaz:
https://doaj.org/article/eb1f20ce524b48c7b06d4716e32203cd
We present an 8-year-old with absence, generalize tonic-clonic and myotonic-atonic seizures who was diagnosed with Doose syndrome based on clinical presentation and EEG findings. A genetic panel found a SUOX gene mutation which has not yet been corre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a45ce57d41ba07bbb35145f3daf39137
https://doi.org/10.22541/au.164493763.39895261/v1
https://doi.org/10.22541/au.164493763.39895261/v1
