Craniosynostosis Syndromes
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Characteristics
- Crouzon syndrome:
- - wide-set, bulging eyes
- - beaked nose
- - flat face
- Apert syndrome
- - fused fingers or toes
- - flat midface
- Loeys-Dietz syndrome
- - wide-set eyes
- - split uvula or cleft palate
- - arterial tortuosity
- - aneurysms
- Muenke syndrome
- - coronal synostosis
- - skeletal abnormalities of the hands or feet
- - hearing loss
- Pfeiffer syndrome
- - broad, short thumbs or big toes
- - webbed or fused fingers or toes
- Saethre-Chotzen syndrome
- - facial asymmetry
- - low frontal hairline
- - drooping eyelids
- - webbed fingers or toes
- - broad big toes
- Shprintzen-Goldberg syndrome
- - bulging eyes - flat face
- - hernias
- - long, thin fingers
- - developmental delay
- - mental retardation
Our Recommendation
If you think that your child has a Craniosynostosis Syndrome, contact us. Professor David has been treating patients with Craniosynostosis Syndromes for over 20 years, with a multidisciplinary, growth to maturity protocol that has been tested on many Australian and International patients.
DDMS Process and Procedure
Professor David, has developed a protocol, in conjunction with the Australian Craniofacial Unit, that incorporates a multidisciplinary approach to treatment. This treatment extends from birth until early adulthood when full development is complete.
Summary
| Locations |
Adelaide |
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| Jakarta |
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| Surabaya |
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| Denpesar - Yayasan Senyum |
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| Sydney |
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| Launceston |
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| Hobart |
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| Kota Bahru |
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| Govt Funded | Medicare Cleft Lip and Palate Scheme |
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