Pallister-Hall syndrome (Q94203): Difference between revisions
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A síndrome de Pallister-Hall é uma síndrome de anomalias congênitas múltiplas caracterizada por uma ampla gama de manifestações clínicas. Associada principalmente a polidactilia central ou pós-axial, sindactilia e hamartoma hipotalâmico. Malformações viscerais são frequentes, tais como atresia anal, úvula bífida, malformações cardíacas congênitas, displasia pulmonar ou renal. | |||
| description / en | description / en | ||
Pallister-Hall syndrome is a multiple congenital anomalies syndrome characterised by a wide range of clinical manifestations. It mainly associates central or postaxial polydactyly, syndactyly, and hypothalamic hamartoma. Visceral malformations are frequent, such as anal atresia, bifid uvula, congenital heart malformations, pulmonary or renal dysplasia. | |||
Revision as of 09:19, 16 August 2026
Pallister-Hall syndrome is a multiple congenital anomalies syndrome characterised by a wide range of clinical manifestations. It mainly associates central or postaxial polydactyly, syndactyly, and hypothalamic hamartoma. Visceral malformations are frequent, such as anal atresia, bifid uvula, congenital heart malformations, pulmonary or renal dysplasia.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1845613381 |
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| English | Pallister-Hall syndrome |
Pallister-Hall syndrome is a multiple congenital anomalies syndrome characterised by a wide range of clinical manifestations. It mainly associates central or postaxial polydactyly, syndactyly, and hypothalamic hamartoma. Visceral malformations are frequent, such as anal atresia, bifid uvula, congenital heart malformations, pulmonary or renal dysplasia. |
