Craniofacial-deafness-hand syndrome (Q59622): Difference between revisions
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A síndrome craniofacial-surdez-mão é definida como a associação de perfil facial plano, hipertelorismo, ausência congênita de ductos nasolacrimais, nariz hipoplásico com narinas em forma de fenda e perda auditiva neurossensorial. | |||
| description / en | description / en | ||
Craniofacial-deafness-hand syndrome is defined as the association of flat facial profile, hypertelorism, congenital absence of nasolacrimal ducts, hypoplastic nose with slit like nares, and a sensorineural hearing loss . | |||
Revision as of 07:08, 14 August 2026
Craniofacial-deafness-hand syndrome is defined as the association of flat facial profile, hypertelorism, congenital absence of nasolacrimal ducts, hypoplastic nose with slit like nares, and a sensorineural hearing loss .
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1355682887 |
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| English | Craniofacial-deafness-hand syndrome |
Craniofacial-deafness-hand syndrome is defined as the association of flat facial profile, hypertelorism, congenital absence of nasolacrimal ducts, hypoplastic nose with slit like nares, and a sensorineural hearing loss . |
