Craniosynostosis
MONDO:0015469Craniosynostosis is defined as the premature fusion of one or more cranial sutures leading to secondary distortion of skull shape resulting in skull deformities with a variable presentation. Craniosynostosis may occur in an isolated setting or as part of a syndrome.
Also known as: craniosynostosis syndrome, premature closure of cranial sutures, CSO
39 clinical trials for this condition and its sub-types, 17 tagged with Craniosynostosis itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Craniosynostosis
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Syndromic craniosynostosis 1 trial · 22 incl. sub-types
40 sub-types
- Acrocephalosyndactyly 0 trials · 13 incl. sub-types Sub-types →
- Crouzon syndrome-acanthosis nigricans syndrome 4 trials
- Antley-Bixler syndrome 2 trials Sub-types →
- Muenke syndrome 2 trials
- Crouzon syndrome 1 trial Sub-types →
- Shprintzen-Goldberg syndrome 1 trial
- Pseudoaminopterin syndrome 1 trial
- Baller-Gerold syndrome 0 trials
- Beare-Stevenson cutis gyrata syndrome 0 trials
- C syndrome 0 trials
- Curry-Jones syndrome 0 trials
- Hunter-McAlpine craniosynostosis 0 trials
- Lowry-MacLean syndrome 0 trials
- Summitt syndrome 0 trials
- TCF12-related craniosynostosis 0 trials
- Weiss-Kruszka syndrome 0 trials
- X-linked intellectual disability-plagiocephaly syndrome 0 trials
- Acrocephalopolydactyly 0 trials
- Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome 0 trials
- Cardiocranial syndrome, Pfeiffer type 0 trials
- Cloverleaf skull-asphyxiating thoracic dysplasia syndrome 0 trials
- Cloverleaf skull-multiple congenital anomalies syndrome 0 trials
- Cranioectodermal dysplasia 0 trials Sub-types →
- Craniomicromelic syndrome 0 trials
- Craniosynostosis 2 0 trials
- Craniosynostosis 4 0 trials
- Craniosynostosis and dental anomalies 0 trials
- Craniosynostosis, Herrmann-Opitz type 0 trials
- Craniosynostosis, Philadelphia type 0 trials
- Craniosynostosis-anal anomalies-porokeratosis syndrome 0 trials
- Craniosynostosis-cataract syndrome 0 trials
- Craniosynostosis-fibular aplasia syndrome 0 trials
- Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome 0 trials
- Craniosynostosis-intracranial calcifications syndrome 0 trials
- Craniotelencephalic dysplasia 0 trials
- Familial scaphocephaly syndrome 0 trials Sub-types →
- Holoprosencephaly-craniosynostosis syndrome 0 trials
- Lethal occipital encephalocele-skeletal dysplasia syndrome 0 trials
- Osteosclerosis-developmental delay-craniosynostosis syndrome 0 trials
- Trigonocephaly-broad thumbs syndrome 0 trials
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Isolated craniosynostosis 1 trial · 3 incl. sub-types
4 sub-types
- Isolated oxycephaly 0 trials · 2 incl. sub-types Sub-types →
- Isolated cloverleaf skull syndrome 0 trials
- Isolated trigonocephaly 0 trials Sub-types →
- Non-syndromic unisutural craniosynostosis 0 trials
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Craniosynostosis syndrome, autosomal recessive 0 trials · 2 incl. sub-types
2 sub-types
- Antley-Bixler syndrome 2 trials Sub-types →
- Cranioectodermal dysplasia 0 trials Sub-types →
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Iida Kannari syndrome 0 trials
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Craniosynostosis Fontaine type 0 trials
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Craniosynostosis autosomal dominant 0 trials
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Craniosynostosis contractures cleft 0 trials
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Craniosynostosis with ectopia lentis 0 trials
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Craniosynostosis, Adelaide type 0 trials
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Mehta lewis patton syndrome 0 trials
Most studied deeper sub-types
Apert syndrome
(11)
Saethre-Chotzen syndrome
(3)
TWIST1-related craniosynostosis
(2)
Pfeiffer syndrome
(1)
Acrocephalopolysyndactyly
(0)
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis
(0)
Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
(0)
Bazopoulou Kyrkanidou syndrome
(0)
Carpenter syndrome
(0)
Cote katsantoni syndrome
(0)
Cranioectodermal dysplasia 1
(0)
Cranioectodermal dysplasia 2
(0)
Cranioectodermal dysplasia 3
(0)
Cranioectodermal dysplasia 4
(0)
Cranioectodermal dysplasia 5
(0)
Cranioectodermal dysplasia 6
(0)
Craniosynostosis 6
(0)
Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome
(0)
Familial scaphocephaly syndrome, McGillivray type
(0)
FGFR1-related Pfeiffer syndrome
(0)