A síndrome de Holt-Oram revisitada: dois casos em uma mesma família / Holt-Oram syndrome revisited: two patients in the same family
Arq. bras. cardiol
;
73(5): 429-34, Nov. 1999. ilus
Article
Dans Portugais, Anglais
| LILACS
| ID: lil-261164
RESUMO
Holt-Oram syndrome was first described in 1960 as an association of familial heart disease and musculoskeletal abnormalities. The most important findings include atrial septal defects, atrioventricular conduction abnormalities, vascular hypoplasia, and upper limb musculoskeletal deformities. We report two patients with this syndrome in the same family and discuss the variability of the musculoskeletal abnormalities and their association with the cardiac morphologic defects. Both patients in this study had associated eosinophilia, which has not been reported in the literature.
Texte intégral:
Disponible
Indice:
LILAS (Amériques)
Sujet Principal:
Pouce
/
Malformations multiples
/
Anomalies morphologiques congénitales de la main
/
Cardiopathies congénitales
Type d'étude:
Etude diagnostique
Limites du sujet:
Adulte
/
Humains
/
Mâle
langue:
Anglais
/
Portugais
Texte intégral:
Arq. bras. cardiol
Thème du journal:
Cardiologie
Année:
1999
Type:
Article
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