Medicine:Brachyturricephaly
From HandWiki
| Brachyturricephaly | |
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| Other names | High prominent forehead High, prominent forehead Turribrachycephaly |
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| Brachyturricephaly in an 8-year-old female with Acrocephalosyndactyly type I | |
Brachyturricephaly is a form of complex craniosynostosis (a combination of brachycephaly and turricephaly) in which the head has both an abnormally high vertical height and a shortened length from anterior to posterior. Malformations of the occipital region are also often present.[1][2][3]
Conditions
Brachyturricephaly is seen in the following conditions:[1]
- Acrocephalosyndactyly type I
- Baller–Gerold syndrome
- Craniofacial dyssynostosis
- Craniosynostosis (nonsyndromic) 2
- Lethal osteosclerotic bone dysplasia
- Microphthalmia with cyst, bilateral facial clefts, and limb anomalies
- Osteogenesis imperfecta type 12
- Peroxisome biogenesis disorder 1A (Zellweger)
- Pfeiffer syndrome
- Shprintzen–Goldberg syndrome
- Uruguay Faciocardiomusculoskeletal syndrome
See also
- List of conditions with craniosynostosis
References
- ↑ 1.0 1.1 "Brachyturricephaly (Concept Id: C1857484)" (in en). https://www.ncbi.nlm.nih.gov/medgen/387833.
- ↑ "Brachyturricephaly - Ontology Browser - Rat Genome Database". https://rgd.mcw.edu/rgdweb/ontology/view.html?acc_id=HP:0000244.
- ↑ Donauer, E.; Bernardy, M.; Neuenfeldt, D. (1993). "T-bone plastique for treatment of brachy-turricephaly". Acta Neurochirurgica 120 (3-4): 126–131. doi:10.1007/BF02112030. ISSN 0001-6268. PMID 8460563. https://pubmed.ncbi.nlm.nih.gov/8460563/.
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