Hyperphalangy (Q46463): Difference between revisions
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| description / pt-br | description / pt-br | ||
A hiperfalangia é uma malformação congênita não sindrômica de membros, caracterizada pela presença de uma falange acessória entre o metacarpo/metatarso e a falange proximal, ou entre quaisquer outras duas falanges de um dedo, excluindo o polegar. A hiperfalangia é quase sempre bilateral e os pacientes não apresentam mais de cinco dígitos nem nenhuma outra anomalia esquelética. | |||
| description / en | description / en | ||
Hyperphalangy is a congenital, non-syndromic limb malformation characterized by the presence of an accessory phalanx between metacarpal/metatarsal and proximal phalanx, or between any two other phalanges of a digit, excluding the thumb. Hypherphalangy is almost always bilateral and patients present no more than five digits and no other skeletal anomalies. | |||
Revision as of 15:03, 13 August 2026
Hyperphalangy is a congenital, non-syndromic limb malformation characterized by the presence of an accessory phalanx between metacarpal/metatarsal and proximal phalanx, or between any two other phalanges of a digit, excluding the thumb. Hypherphalangy is almost always bilateral and patients present no more than five digits and no other skeletal anomalies.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LB77 |
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| English | Hyperphalangy |
Hyperphalangy is a congenital, non-syndromic limb malformation characterized by the presence of an accessory phalanx between metacarpal/metatarsal and proximal phalanx, or between any two other phalanges of a digit, excluding the thumb. Hypherphalangy is almost always bilateral and patients present no more than five digits and no other skeletal anomalies. |
