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Familial Hirschsprung's disease and type D brachydactyly: a report of four affected males in two generations.
Pediatrics ; 71(2): 246-9, 1983 Feb.
Article em En | MEDLINE | ID: mdl-6823428
Hirschsprung's disease usually occurs as an isolated malformation as a result of multifactorial causation. A family in which four males (two brothers and two maternal uncles) had Hirschsprung's disease and absence or hypoplasia of the nails and distal phalanges of the great toe and thumb (type D brachydactyly) is described. Hand abnormalities were not present in any other family members, and the obligate heterozygous females were without gastrointestinal problems. The pattern of inheritance was consistent with X-linked recessive inheritance; however, autosomal dominant inheritance with incomplete penetrance in females or multifactorial causation could not be completely excluded.
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Hirschsprung / Unhas Malformadas Limite: Adolescent / Adult / Child / Child, preschool / Humans / Infant / Male / Newborn Idioma: En Revista: Pediatrics Ano de publicação: 1983 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Hirschsprung / Unhas Malformadas Limite: Adolescent / Adult / Child / Child, preschool / Humans / Infant / Male / Newborn Idioma: En Revista: Pediatrics Ano de publicação: 1983 Tipo de documento: Article