Thomas syndrome: potter sequence with cleft lip/palate and cardiac anomalies.
Am J Med Genet
; 62(3): 224-6, 1996 Mar 29.
Article
em En
| MEDLINE
| ID: mdl-8882777
ABSTRACT
Holzgreve et al. [Am J Med Genet 18177-184, 1984] first reported on a syndrome including renal anomalies, heart defect, polydactyly, and cleft palate with other oropharyngeal anomalies. We report here on four sibs with renal adysplasia associated in two with cardiovascular malformations and cleft lip or cleft palate in two. We propose that these patients as the two siblings reported by Thomas et al. [Am J Med Genet 45767-769, 1993] are affected with a syndrome different of the one described by Holzgreve et al. [Am J Med Genet 18177-184, 1984] mainly because of the absence of polydactyly. Thomas syndrome is probably inherited as an autosomal recessive trait with marked variability.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Palato
/
Anormalidades Múltiplas
/
Fenda Labial
/
Cardiopatias Congênitas
/
Rim
Tipo de estudo:
Diagnostic_studies
Limite:
Adult
/
Female
/
Humans
/
Male
/
Newborn
/
Pregnancy
Idioma:
En
Revista:
Am J Med Genet
Ano de publicação:
1996
Tipo de documento:
Article
País de afiliação:
Israel