Overview
Turricephaly is a type of cephalic disorder where the head appears tall with a small length and width. It is due to premature closure of the coronal suture plus any other suture, like the lambdoid, or it may be used to describe the premature fusion of all sutures. 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.
Presentation
Common associations
It may be associated with:
8th cranial nerve lesion
Optic nerve compression
Intellectual disability
Syndactyly
Conditions with turricephaly
Conditions with turricephaly include:
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
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
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