Robinow-Sorauf syndrome (Q93982): Difference between revisions
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A síndrome de Robinow-Sorauf é uma síndrome de craniossinostose caracterizada por craniossinostose, plagiocefalia, face plana, hipertelorismo, nariz fino, longo e pontudo, órbitas rasas, estrabismo e dedões grandes dos pés com uma duplicação da falange distal. | |||
| description / en | description / en | ||
Robinow-Sorauf syndrome is a craniosynostosis syndrome characterised by craniosynostosis, plagiocephaly, flat face, hypertelorism, a thin, long, and pointed nose, shallow orbits, strabismus, and broad great toes with a duplication of the distal phalanx. | |||
Revision as of 09:05, 16 August 2026
Robinow-Sorauf syndrome is a craniosynostosis syndrome characterised by craniosynostosis, plagiocephaly, flat face, hypertelorism, a thin, long, and pointed nose, shallow orbits, strabismus, and broad great toes with a duplication of the distal phalanx.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1272297510 |
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| English | Robinow-Sorauf syndrome |
Robinow-Sorauf syndrome is a craniosynostosis syndrome characterised by craniosynostosis, plagiocephaly, flat face, hypertelorism, a thin, long, and pointed nose, shallow orbits, strabismus, and broad great toes with a duplication of the distal phalanx. |
