Brachyturricephaly
| Brachyturricephaly | |
|---|---|
| Other names | High prominent forehead High, prominent forehead Turribrachycephaly |
 | |
| Brachyturricephaly in an 8-year-old female with Acrocephalosyndactyly type I | |
Brachyturricephaly is a form of complex
Conditions
Brachyturricephaly is seen in the following conditions:[1]
- Acrocephalosyndactyly type I
- Baller–Gerold syndrome
- Craniofacial dyssynostosis
- Craniosynostosis (nonsyndromic) 2
- Lethal osteosclerotic bone dysplasia
- facial clefts, and limb anomalies
- Osteogenesis imperfecta type 12
- Peroxisome biogenesis disorder 1A (Zellweger)
- Pfeiffer syndrome
- Shprintzen–Goldberg syndrome
- Uruguay Faciocardiomusculoskeletal syndrome
See also
References
- ^ a b "Brachyturricephaly (Concept Id: C1857484)". www.ncbi.nlm.nih.gov. Retrieved 2023-10-14.
- ^ "Brachyturricephaly - Ontology Browser - Rat Genome Database". rgd.mcw.edu. Retrieved 2023-10-14.
- PMID 8460563.