메뉴 건너뛰기
.. 내서재 .. 알림
소속 기관/학교 인증
인증하면 논문, 학술자료 등을  무료로 열람할 수 있어요.
한국대학교, 누리자동차, 시립도서관 등 나의 기관을 확인해보세요
(국내 대학 90% 이상 구독 중)
로그인 회원가입 고객센터 ENG
주제분류

추천
검색

이용수

표지
📌
연구주제
📖
연구배경
🔬
연구방법
🏆
연구결과
AI에게 요청하기
추천
검색

초록· 키워드

오류제보하기
The familial periodic paralysis (FPP) is a rare inherited channelopathy characterized by reversible attacks of muscle weakness. It has been commonly considered to be a benign disease since frequency and severity of the paralytic attacks improve in adulthood. However, with increasing age, a portion of the patients develops permanent weakness and this may be explained by a progressive destruction of muscle tissue. We report a 19 year-old man who had been showing permanent weakness after recurrent paralytic attacks, which began in late childhood. Along with periodic paralysis, he also exhibited cardiac arrhythmia and dysmorphic features. Clinical diagnosis of Andersen-Tawil syndrome was done by these triad. Up to now there are many reports of FPP in Korea, but few or no studies of permanent weakness were reported, especially in young age. We report atypical case of FPP with early onset of permanent weakness.

목차

등록된 정보가 없습니다.

참고문헌 (9)

참고문헌 신청

이 논문의 저자 정보

최근 본 자료

전체보기

댓글(0)

0