Raynaud-Claes Sendromu; ketojenik diyet hayat kurtarıcı olabilir
Abstract
Keywords
References
- 1. He H, Guzman RE, Cao D, Sierra-Marquez J, Yin F, Fahlke C, et al. The molecular and phenotypic spectrum of CLCN4-related epilepsy. Epilepsia. 2021;62(6):1401-1415. 2. Xu X, Lu F, Zhang L, Li H, Du S, Tang J. Novel CLCN4 variant associated withsyndromic X-linked intellectual disability in a Chinese girl: a case report. BMC Pediatr. 2021;3;21(1):384.
- 2. Weinert S, Gimber N, Deuschel D et al. Uncouplingendosomal CLC chloride/proton exchange causes severe neurodegeneration. EMBO J. 2020;4;39(9):e103358.
- 3. Zhou P, He N, Zhang JW et al. Novel mutations and phenotypes of epilepsy-associated genes in epileptic encephalopathies. Genes Brain Behav. 2018;17(8):e12456.
- 4. Archila R, Papazian O. Síndrome de Lennox-Gastaut [Lennox-Gastaut syndrome]. Rev Neurol. 1999;16-31;29(4):346-9. 5. Accardi A, Miller C. Secondary active transport mediated by a prokaryotichomologue of ClC Cl- channels. Nature. 2004:26; 427 (6977) :803-7.
Details
Primary Language
Turkish
Subjects
Health Care Administration
Journal Section
Case Report
Publication Date
June 30, 2022
Submission Date
February 10, 2022
Acceptance Date
March 10, 2022
Published in Issue
Year 2022 Volume: 15 Number: (Özel Sayı-1) 21. Mersin Pediatri Günleri Bildiri Kitabı
