1.
Rev. Hosp. Säo Paulo Esc. Paul. Med
;
2(3/4): 79-82, July-Dec. 1990. ilus, tab
Article
in English
| LILACS
| ID: lil-140658
ABSTRACT
We report on a Brazilian family with six affected patients, in two generations, which presented flat face and feet anomalies ranging from mild metatarsus varus to severe clubfoot. Autosomal dominant pattern of inheritance can be demonstrated. Clinical and genetical aspects are discussed
Subject(s)
Child, Preschool , Child , Adolescent , Adult , Humans , Male , Female , Abnormalities, Multiple/genetics , Joint Dislocations/genetics , Face/abnormalities , Talipes/genetics , Pedigree , Syndrome
2.
Rev. bras. genét
;
6(1): 93-9, 1983.
Article
in English
| LILACS
| ID: lil-17558
ABSTRACT
Foi estudada uma crianca brasileira de sexo masculino, nascida de casal consanguineo e apresentando as caracteristicas tipicas da sindrome de Schwartz, bem como anomalia eletrocardiografica (sindrome de Lown-Ganong-Levine), sinais de insuficiencia cardiaca congestiva e anormalidades dentarias. Sao discutidos aspectos clinicos e geneticos