Create issue ticket

405 Possible Causes for Coronal Craniosynostosis

  • Craniofrontonasal Dysplasia

    Craniofrontonasal dysplasia's (CFND's) phenotypic range includes hypertelorism, coronal craniosynostosis, frontonasal dysplasia, and digital anomalies.[ncbi.nlm.nih.gov] Coronal craniosynostosis, hypertelorism, telecanthus, broad grooved nasal tip, dental anomalies, mild syndactyly and broad thumbs, consistent with craniofrontonasal dysplasia[ncbi.nlm.nih.gov] craniosynostosis, various digital and limb anomalies including syndactyly, clinodactyly of the 5th finger, broad thumbs) and ectodermal dysplasias (dental anomalies, grooved[orpha.net]

  • Craniosynostosis

    Coronal Craniosynostosis Coronal Craniosynostosis is a premature closure of the skull sutures that lie behind the forehead and run from side to side.[rchsd.org] Although pathological expression of these mutations often results in bilateral coronal craniosynostosis, single suture fusions (typically unilateral coronal synostosis) or[ncbi.nlm.nih.gov] , which include testing nonsyndromic cases of sagittal, metopic, and coronal craniosynostosis.[ncbi.nlm.nih.gov]

  • Baller-Gerold Syndrome

    The coronal craniosynostosis that is commonly seen in patients with BGS results in the fusion of the skull along the coronal suture.[en.wikipedia.org] Twin A had severe coronal craniosynostosis. Twin B had right radioulnar and ipsilateral first metacarpal hypoplasia. Both had bilateral fifth finger clinodactyly.[ncbi.nlm.nih.gov] […] syndrome which is characterized by coronal craniosynostosis usually without radial ray anomalies (see these terms).[orpha.net]

  • Craniosytosis Type 4

    Louis Children’s Hospital treat coronal synostosis and all other types of craniosynostosis in infants. What is Coronal Synostosis?[stlouischildrens.org] Coronal synostosis: Coronal synostosis is the most common suture demonstrated in syndromic craniosynostosis. It is more likely to be bilateral.[ispn.guide] The cause of coronal nonsyndromic craniosynostosis is not well understood, although the published literature suggests that it is a multi-factorial condition.[labs.icahn.mssm.edu]

  • Craniosynostosis Type 3

    craniosynostosis model.[agris.fao.org] Closure of a single coronal suture is called unilateral coronal craniosynostosis or unicoronal craniosynostosis.[drderderian.com] […] trigonocephaly (wedge shaped) unilateral coronal craniosynostosis bilateral cornoal craniosynostosis posterior or occipital plagiocephaly sagittal craniosynostosis unilateral[brainscape.com]

  • Gorlin-Chaudhry-Moss Syndrome

    Clinical description GCM is a congenital disorder in which patients present with a stocky body build, normal intelligence, coronal craniosynostosis, facial dysmorphism (brachy[rarediseases.info.nih.gov]

  • Apert Syndrome

    Apert syndrome is a rare disorder characterized by coronal craniosynostosis, syndactyly, brachycephaly, midfacial hypoplasia, and central nervous system anomalies, among other[ncbi.nlm.nih.gov] Apert syndrome is characterized by coronal craniosynostosis, midfacial hypoplasia, symmetrical syndactyly of the hands and feet described as 'mitten-like' with varying degrees[ncbi.nlm.nih.gov] craniosynostosis, symmetric bone and skin syndactyly of hands and feet, and craniofacial dysmorphic features.[ncbi.nlm.nih.gov]

  • Familial Scaphocephaly Syndrome

    Bilateral coronal craniosynostosis, the most common syndromic form, causes a short and wide head.[neurosurgery.ufl.edu] Unilateral Coronal Craniosynostosis Unilateral coronal craniosynostosis (frontal plagiocephaly) is the second most common form of craniosynostosis.[hopkinsallchildrens.org] Coronal Craniosynostosis (plagiocephaly) Coronal Craniosynostosis is a premature closure of the skull sutures that lie behind the forehead and run from side to side.[craniofacialmd.com]

  • Saethre-Chotzen Syndrome

    We recommend screening for a deletion of the TWIST1 gene if signs of coronal craniosynostosis with no clear etiology are observed on ultrasound examination.[ncbi.nlm.nih.gov] Finally, since no TWIST mutations were detected in 40 cases of isolated coronal craniosynostosis, the present study suggests that TWIST mutations are specific to Saethre-Chotzen[ncbi.nlm.nih.gov] Craniosynostosis of one or both coronal craniosynostosis Asymmetric skulls and facial features Eyelid Ptosis An Accentuated Crease in the ear Low frontal hairline[childrens.com]

  • Craniosynostosis-Dandy-Walker Malformation-Hydrocephalus Syndrome

    Home Documents Semilobar holoprosencephaly, coronal craniosynostosis, and multiple congenital anomalies: A severe expression of the Genoa syndrome or a newly recognized syndrome[dev.docslide.net] Dysplasia, San Diego Type Spondyloepiphyseal Dysplasia with Coronal Craniosynostosis, Cataracts, Cleft Palate, and Mental Retardation syndromic X-linked intellectual disability[rgd.mcw.edu] Note down-slanting palpebralfissures, midfacial hypoplasia, coronal craniosynostosis, low-set ears, facialasymmetry, and prominent metopic fontanel.[docslide.com.br]

Further symptoms