Turricephaly
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| Turricephaly | |
|---|---|
| Other names | Oxycephaly,[1] Acrocephaly, Hypsicephaly,[1] Oxycephalia,[1] Steeple head,[1] Tower head,[1] Tower skull, High-head syndrome, Turmschädel[2] |
| File:Turricephaly.jpg | |
| Specialty | Dysmorphology |
| Symptoms | reduced head length and width for age |
Turricephaly is a type of cephalic disorder where the head appears tall with a small length and width.[3][4] It is due to premature closure of the coronal suture plus any other suture, like the lambdoid,[5] or it may be used to describe the premature fusion of all sutures.[2] It should be differentiated from Crouzon syndrome. Oxycephaly (or acrocephaly) is a form of turricephaly where the head is cone-shaped, and is the most severe of the craniosynostoses.[4]
Presentation
[edit | edit source]Common associations
[edit | edit source]It may be associated with:[6]
Conditions with turricephaly
[edit | edit source]Conditions with turricephaly include:[7][8]
- Achondrogenesis, type IA
- Acrocephalopolydactyly
- Acrocephalosyndactyly type V (Goodman syndrome)
- Acrocraniofacial dysostosis
- Alopecia - contractures - dwarfism - intellectual disability syndrome
- CEBALID syndrome
- Chromosome 1q21.1 deletion syndrome
- Chromosome 4q32.1-q32.2 triplication syndrome
- Chromosome 5p13 duplication syndrome
- Cole-Carpenter syndrome 2
- Craniorhiny
- Craniosynostosis (nonsyndromic) 6
- Craniosynostosis, Boston-type (nonsyndromic)
- Craniosynostosis and dental anomalies
- Fontaine progeroid syndrome
- Gomez Lopez Hernandez syndrome
- Intellectual developmental disorder, autosomal dominant 65
- MEGF8-related Carpenter syndrome
- Mosaic trisomy 12[9]
- Myopathy, epilepsy, and progressive cerebral atrophy
- Peroxisome biogenesis disorder 2A (Zellweger)
- Potocki-Shaffer syndrome
- Saethre-Chotzen syndrome
- Spondyloenchondrodysplasia with immune dysregulation
- Spondylometaphyseal dysplasia, Sedaghatian type
- Summitt syndrome
- Teebi-Shaltout syndrome
- Tolchin-Le Caignec syndrome
- TWIST1-related craniosynostosis
- Usmani-Riazuddin syndrome, autosomal dominant
-
Carpenter syndrome
-
Saethre-Chotzen syndrome
Diagnosis
[edit | edit source]| [icon] | This section is empty. You can help by adding to it. (February 2018) |
Treatment
[edit | edit source]| [icon] | This section is empty. You can help by adding to it. (February 2018) |
See also
[edit | edit source]References
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Further reading
[edit | edit source]- NINDS Overview
- Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
External links
[edit | edit source]Look up oxycephaly in Wiktionary, the free dictionary.