Catalog
Syndromic craniosynostoses
Link to WHO Definition
Syndromic craniosynostoses – http://id.who.int/icd/entity/1908604930
Any syndrome caused by premature fusing of sections of the infant skull. These syndromes are characterised by disfiguring compensatory growth of the skull. These syndromes may also present with frequent worsening morning headache, recurrent vomiting, cephalocranial disproportion, raised intracranial pressure, optic atrophy, blindness, or developmental delay.
Parents
Children
- LD24.G0 Pfeiffer syndrome
- Robinow-Sorauf syndrome
- Hunter-McAlpine craniosynostosis
- C syndrome
- Cloverleaf skull - asphyxiating thoracic dysplasia
- LD24.G1 Crouzon disease
- Craniosynostosis, Boston type
- Baller-Gerold syndrome
- Craniomicromelic syndrome
- Aurocephalosyndactyly
- Muenke syndrome
- LD24.G2 Apert syndrome
- Antley-Bixler syndrome
- Craniosynostosis, Herrmann-Opitz type
- Saethre-Chotzen syndrome
- Carpenter syndrome
- Craniosynostosis, Philadelphia type
- Familial scaphocephaly syndrome, McGillivray type
- Crouzon syndrome - acanthosis nigricans
- Craniofrontonasal dysplasia
- Pseudoaminopterin syndrome