Jervell : KMLE 의학 검색 엔진 - 의학사전, 의학용어, 의학약어, 의학논문, 약품/의약품 검색

KMLE 웹 용어 맞춤 검색 결과 : 2 페이지: 1

Jervell and Lange-Nielsen syndrome	A genetic syndrome or profound congenital deafness associated with syncope (fainting) secondary to a heart conduction defect. Distinguishing this specific etiology (cause) for deafness is important, because drug treatment may prevent sudden death during a syncopal episode. Incidence is 1 in 1 million, with an autosomal recessive inheritance pattern. 출처: www.childrenwithchallenges.net/definitions/J.html
Jervell and Lange-Nielsen s.	an autosomal recessive form of the long QT syndrome, characterized by neural deafness and syncope, and sometimes ventricular fibrillation and sudden death. Cf. Romano-Ward s. 출처: www.mercksource.com/pp/us/cns/cns_health_library.j...

Jervell and Lange-Nielsen syndrome

A genetic syndrome or profound congenital deafness associated with syncope (fainting) secondary to a heart conduction defect. Distinguishing this specific etiology (cause) for deafness is important, because drug treatment may prevent sudden death during a syncopal episode. Incidence is 1 in 1 million, with an autosomal recessive inheritance pattern.

출처: www.childrenwithchallenges.net/definitions/J.html

Jervell and Lange-Nielsen s.

an autosomal recessive form of the long QT syndrome, characterized by neural deafness and syncope, and sometimes ventricular fibrillation and sudden death. Cf. Romano-Ward s.

출처: www.mercksource.com/pp/us/cns/cns_health_library.j...