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Arch Pediatr Adolesc Med ; 159(9): 876-81, 2005 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16143748

RESUMO

OBJECTIVE: To describe families with multiple members affected with Kawasaki syndrome (KS) to increase awareness of the familial occurrence of KS among practitioners who care for these patients. DESIGN: Retrospective review of medical records at 2 medical centers and data collection from remote KS families who contacted the KS Research Program at the University of California, San Diego. RESULTS: Eighteen families with multiple affected members were identified. There were 9 families with 2 affected siblings. In San Diego, 3 (0.7%) of 424 KS families had sibling cases. Nine families were identified with KS in 2 generations or in multiple affected members, yielding a total of 24 KS-affected children. No clear pattern of inheritance could be deduced from these pedigrees, and it is likely that multiple polymorphic alleles influence KS susceptibility. CONCLUSION: Physicians should counsel affected families and make them aware of the potential increased risk of KS among family members.


Assuntos
Asiático/genética , Família/etnologia , Síndrome de Linfonodos Mucocutâneos/epidemiologia , Síndrome de Linfonodos Mucocutâneos/genética , Linhagem , Adolescente , Povo Asiático/genética , Boston/epidemiologia , California/epidemiologia , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Recém-Nascido , Masculino , Americanos Mexicanos/genética , América do Norte/epidemiologia , Prevalência , Fatores de Risco , Irmãos/etnologia , População Branca/genética
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