A Study of the Inheritance Pattern of Romano-Ward Syndrome
- 1 January 1982
- journal article
- other
- Published by SAGE Publications in Clinical Pediatrics
- Vol. 21 (1) , 20-24
- https://doi.org/10.1177/000992288202100103
Abstract
Romano-Ward syndrome consists of attacks of syncope, possible sudden death, accompanied by prolonged Q-T interval on ECG. We carried out HLA antigen typing of a family of 16 members having ten cases of Romano-Ward syndrome. All the ten cases had the common HLA haplotype of A9-Bw54, while the six not showing the symptoms did not have A9-Bw54 haplotype. The genes of this syndrome, considered to be inherited through the autosomal dominant patterns, are assumed to have a close linking to the major histo compatibility complex on the short arm of chromosome number 6.Keywords
This publication has 14 references indexed in Scilit:
- Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden deathPublished by Elsevier ,2004
- Genetic Mapping of Ir Locus in Man: Linkage to Second Locus of HL-AScience, 1974
- Ragweed Hay Fever: Genetic Control and Linkage to HL-A HaplotypesScience, 1972
- Q-T Prolongation and ventricular arrhythmias, with and without deafness, in the same familyThe American Journal of Cardiology, 1972
- Histocompatibility-Linked Immune Response GenesScience, 1972
- QT-Interval Prolongation, Paroxysmal Ventricular Arrhythmias, and Convulsive SyncopeAnnals of Internal Medicine, 1971
- Syncope and Q-T prolongation without deafness: The Romano-Ward syndromeAmerican Heart Journal, 1970
- Hereditary prolongation of QT interval: Study of two familiesHeart, 1970
- UNEXPECTED COT DEATHSThe Lancet, 1966
- CONGENITAL CARDIAC ARRHYTHMIAThe Lancet, 1964