Greig cephalopolysyndactyly syndrome (Q84223): Difference between revisions
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| description / pt-br | description / pt-br | ||
A síndrome cefalopolissindactilia de Greig é uma síndrome de anomalia congênita múltipla pleiotrópica caracterizada por hipertelorismo, macrocefalia com protusão frontal e polissindactilia mais comumente pré-axial nos pés e pós-axial nas mãos. | |||
| description / en | description / en | ||
Greig cephalopolysyndactyly syndrome is a pleiotropic, multiple congenital anomaly syndrome characterised by hypertelorism, macrocephaly with frontal bossing, and polysyndactyly most commonly preaxial in the feet and postaxial in the hands. | |||
Revision as of 09:34, 15 August 2026
Greig cephalopolysyndactyly syndrome is a pleiotropic, multiple congenital anomaly syndrome characterised by hypertelorism, macrocephaly with frontal bossing, and polysyndactyly most commonly preaxial in the feet and postaxial in the hands.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_606500237 |
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| English | Greig cephalopolysyndactyly syndrome |
Greig cephalopolysyndactyly syndrome is a pleiotropic, multiple congenital anomaly syndrome characterised by hypertelorism, macrocephaly with frontal bossing, and polysyndactyly most commonly preaxial in the feet and postaxial in the hands. |
