Carpenter syndrome (Q93994): Difference between revisions
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A síndrome de Carpenter é um subtipo de uma família de transtornos genéticos conhecidos como transtornos da acrocefalopolissindactilia (ACPS). É definida por acrocefalia, fácies peculiar, braquidactilia e sindactilia nas mãos e polidactilia e sindactilia pré-axial dos dedos dos pés. | |||
| description / en | description / en | ||
Carpenter syndrome is a subtype of a family of genetic disorders known as acrocephalopolysyndactyly (ACPS) disorders. It is defined by acrocephaly, peculiar facies, brachydactyly and syndactyly in the hands, and preaxial polydactyly and syndactyly of the toes. | |||
Revision as of 09:06, 16 August 2026
Carpenter syndrome is a subtype of a family of genetic disorders known as acrocephalopolysyndactyly (ACPS) disorders. It is defined by acrocephaly, peculiar facies, brachydactyly and syndactyly in the hands, and preaxial polydactyly and syndactyly of the toes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2132713612 |
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| English | Carpenter syndrome |
Carpenter syndrome is a subtype of a family of genetic disorders known as acrocephalopolysyndactyly (ACPS) disorders. It is defined by acrocephaly, peculiar facies, brachydactyly and syndactyly in the hands, and preaxial polydactyly and syndactyly of the toes. |
