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Clinical and Genetic Features of Congenital Myasthenic Syndromes due to CHAT Mutations: Case Report and Literature Review.
Arican, Pinar; Gencpinar, Pinar; Cavusoglu, Dilek; Olgac Dundar, Nihal.
Afiliación
  • Arican P; Department of Pediatric Neurology, Izmir Tepecik Education and Research Hospital, Izmir, Turkey.
  • Gencpinar P; Department of Pediatric Neurology, Izmir Katip Celebi University, Izmir, Turkey.
  • Cavusoglu D; Department of Pediatric Neurology, Afyon Kocatepe University, Afyon, Turkey.
  • Olgac Dundar N; Department of Pediatric Neurology, Izmir Katip Celebi University, Izmir, Turkey.
Neuropediatrics ; 49(4): 283-288, 2018 08.
Article en En | MEDLINE | ID: mdl-29783273
Congenital myasthenic syndromes (CMS) are neuromuscular transmission disorders caused by mutations in genes encoding neuromuscular junction proteins. CMS due to choline acetyltransferase (CHAT) gene is characterized by episodic apnea. We report a case of a 12-month-old female patient presented with recurrent episodic apnea carrying a mutation in CHAT gene, p.I336T. Furthermore, we describe the genetic and clinical findings in 44 CMS patients due to CHAT mutations in the literature up to date. Episodes of apnea and respiratory insufficiency are the hallmarks of CHAT mutations. Clinical manifestations usually provoked by infections and fever. CMS due to CHAT mutations are rare, but it is important to diagnosis. Early diagnosis and appropriate treatment can improve morbidity and mortality.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Colina O-Acetiltransferasa / Síndromes Miasténicos Congénitos / Mutación Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Female / Humans / Infant Idioma: En Revista: Neuropediatrics Año: 2018 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Colina O-Acetiltransferasa / Síndromes Miasténicos Congénitos / Mutación Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Female / Humans / Infant Idioma: En Revista: Neuropediatrics Año: 2018 Tipo del documento: Article País de afiliación: Turquía