| Jervell and Lange-Nielsen syndrome | <syndrome> A prolonged Q-T interval recorded in the electrocardiogram of certain congenitally deaf children subject to attacks of unconsciousness resulting from Adams-Stokes seizures and ventricular fibrillation; autosomal recessive inheritance. Synonym: surdocardiac syndrome. (05 Mar 2000) |
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| Jervell, Anton | <person> 20th century Norwegian cardiologist. See: Jervell and Lange-Nielsen syndrome. (05 Mar 2000) |
Synonyms : Jervell and Lange-Nielsen Syndrome, Jervell Lange Nielsen Syndrome, Jervell and Lange Nielsen Syndrome, Nielsen Syndrome, Jervell-Lange, Syndrome, Jervell-Lange Nielsen
| 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.
Ãâó: www.childrenwithchallenges.net/definitions/J.html
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| 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.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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