Osteochondrodysplatic nanism - deafness - retinitis pigmentosa (Q67452): Difference between revisions
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Síndrome de nanismo osteocondrodisplático - surdez - retinite pigmentosa é caracterizada por nanismo grave, escoliose progressiva e luxação bilateral do quadril, associada a surdez neurossensorial e retinite pigmentosa. | |||
| description / en | description / en | ||
Osteochondrodysplatic nanism - deafness - retinitis pigmentosa syndrome is characterised by severe dwarfism, progressive scoliosis and bilateral dislocation of the hip, associated with sensorineural deafness and retinitis pigmentosa. | |||
Revision as of 15:16, 14 August 2026
Osteochondrodysplatic nanism - deafness - retinitis pigmentosa syndrome is characterised by severe dwarfism, progressive scoliosis and bilateral dislocation of the hip, associated with sensorineural deafness and retinitis pigmentosa.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1095798962 |
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| English | Osteochondrodysplatic nanism - deafness - retinitis pigmentosa |
Osteochondrodysplatic nanism - deafness - retinitis pigmentosa syndrome is characterised by severe dwarfism, progressive scoliosis and bilateral dislocation of the hip, associated with sensorineural deafness and retinitis pigmentosa. |
