Academic Journal

First Molecular Diagnosis of a Patient with Unverricht-Lundborg Disease in Korea

التفاصيل البيبلوغرافية
العنوان: First Molecular Diagnosis of a Patient with Unverricht-Lundborg Disease in Korea
المساهمون: College of Medicine, Dept. of Neurology, Ki Hoon Kim, Ju Sun Song, Chan Wook Park, Chang-Seok Ki, Kyoung Heo, Park, Chan Wook, Heo, Kyoung
بيانات النشر: Yonsei University
سنة النشر: 2018
مصطلحات موضوعية: Adult, Anticonvulsants/administration & dosage, Anticonvulsants/therapeutic use, Blotting, Southern, Cystatin B/genetics, Female, Genetic Predisposition to Disease, Humans, Isoxazoles/administration & dosage, Isoxazoles/therapeutic use, Piracetam/administration & dosage, Piracetam/analogs & derivatives, Piracetam/therapeutic use, Republic of Korea, Seizures/physiopathology, Treatment Outcome, Unverricht-Lundborg Syndrome/diagnosis, Unverricht-Lundborg Syndrome/drug therapy, Unverricht-Lundborg Syndrome/genetics, Valproic Acid/administration & dosage, Valproic Acid/therapeutic use, Progressive myoclonic epilepsy, Southern blot, Unverricht-Lundborg disease
الوصف: Unverricht-Lundborg disease (ULD) is a form of progressive myoclonus epilepsy characterized by stimulation-induced myoclonus and seizures. This disease is an autosomal recessive disorder, and the gene CSTB, which encodes cystatin B, a cysteine protease inhibitor, is the only gene known to be associated with ULD. Although the prevalence of ULD is higher in the Baltic region of Europe and the Mediterranean, sporadic cases have occasionally been diagnosed worldwide. The patient described in the current report showed only abnormally enlarged restriction fragments of 62 dodecamer repeats, confirming ULD, that were transmitted from both her father and mother who carried the abnormally enlarged restriction fragment as heterozygotes with normal-sized fragments. We report the first case of a genetically confirmed patient with ULD in Korea. ; open
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
تدمد: 0513-5796
1976-2437
Relation: YONSEI MEDICAL JOURNAL; J02813; OAK-2018-03213; https://ir.ymlib.yonsei.ac.kr/handle/22282913/163136; T201802209; YONSEI MEDICAL JOURNAL, Vol.59(6) : 798-800, 2018; 58407
DOI: 10.3349/ymj.2018.59.6.798
الاتاحة: https://ir.ymlib.yonsei.ac.kr/handle/22282913/163136
https://doi.org/10.3349/ymj.2018.59.6.798
Rights: CC BY-NC-ND 2.0 KR ; https://creativecommons.org/licenses/by-nc-nd/2.0/kr/
رقم الانضمام: edsbas.A6ECEBA7
قاعدة البيانات: BASE
الوصف
تدمد:05135796
19762437
DOI:10.3349/ymj.2018.59.6.798