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{{Infobox medical condition |
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|name = Craniorhiny |
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|synonyms = <!-- or |synonym= --> |
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|image = Autodominant.jpg |
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|image_size = 230px |
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|caption = Autosomal dominant inheritance |
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'''Craniorhiny''' is a rare [[autosomal dominant]] syndrome characterized by [[craniosynostosis]] ([[oxycephaly]]) and facial anomalies around the nose base and lips. |
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== Signs and symptoms == |
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Features of this condition include: |
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* Head or neck: anteverted [[nares]], wide nose |
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* Integument: [[hirsutism]] |
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* Musculoskeletal system: craniosynotosis, oxycephaly/turricephaly |
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== History == |
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The first (and only confirmed) reports of this condition was made in 1991, seen in a father and son. Two siblings reported in 2007 are also speculated to have the condition. |
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Revision as of 15:59, 16 September 2023
| Craniorhiny | |
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| Autosomal dominant inheritance |
Craniorhiny is a rare autosomal dominant syndrome characterized by craniosynostosis (oxycephaly) and facial anomalies around the nose base and lips.
Signs and symptoms
Features of this condition include:
- Head or neck: anteverted nares, wide nose
- Integument: hirsutism
- Musculoskeletal system: craniosynotosis, oxycephaly/turricephaly
History
The first (and only confirmed) reports of this condition was made in 1991, seen in a father and son. Two siblings reported in 2007 are also speculated to have the condition.