Weissenbacher- Zweymuller syndrome (Q88326): Difference between revisions
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A síndrome de Weissenbacher-Zweymuller é uma doença genética caracterizada por baixa estatura ao nascimento, micrognatia neonatal, fenda palatina, condrodisplasia rizomélica com ossos do braço e perna em formato de halteres, hipertelorismo e fendas coronais vertebrais. | |||
| description / en | description / en | ||
Weissenbacher-Zweymuller syndrome is a genetic disorder characterised by short stature at birth, neonatal micrognathia, cleft palate, rhizomelic chondrodysplasia with 'dumbbell' shaped arm and leg bones, hypertelorism and vertebral coronal clefts. | |||
Revision as of 14:31, 15 August 2026
Weissenbacher-Zweymuller syndrome is a genetic disorder characterised by short stature at birth, neonatal micrognathia, cleft palate, rhizomelic chondrodysplasia with 'dumbbell' shaped arm and leg bones, hypertelorism and vertebral coronal clefts.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1421501711 |
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| English | Weissenbacher- Zweymuller syndrome |
Weissenbacher-Zweymuller syndrome is a genetic disorder characterised by short stature at birth, neonatal micrognathia, cleft palate, rhizomelic chondrodysplasia with 'dumbbell' shaped arm and leg bones, hypertelorism and vertebral coronal clefts. |
