Fibrochondrogenesis (Q88325): Difference between revisions
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| description / pt-br | description / pt-br | ||
A fibrocondrogênese é uma rara condrodisplasia rizomélica, letal no período neonatal, caracterizada por uma face característica com olhos protuberantes, face plana na linha mediana, nariz pequeno achatado com narinas antevertidas e uma boca pequena com lábio superior longo. | |||
| description / en | description / en | ||
Fibrochondrogenesis is a rare, neonatally lethal, rhizomelic chondrodysplasia and is characterised by a distinctive face with protuberant eyes, flat midface, flat small nose with anteverted nares and a small mouth with long upper lip. | |||
Revision as of 14:31, 15 August 2026
Fibrochondrogenesis is a rare, neonatally lethal, rhizomelic chondrodysplasia and is characterised by a distinctive face with protuberant eyes, flat midface, flat small nose with anteverted nares and a small mouth with long upper lip.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1412541453 |
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| English | Fibrochondrogenesis |
Fibrochondrogenesis is a rare, neonatally lethal, rhizomelic chondrodysplasia and is characterised by a distinctive face with protuberant eyes, flat midface, flat small nose with anteverted nares and a small mouth with long upper lip. |
