Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. It is classified...
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Craniosynostosis (redirect from Sagittal craniosynostosis syndrome)
Shprintzen-Goldberg syndrome: craniosynostosis with marfanoid habitus and tissue anomalies. Apert syndrome Carpenter syndrome Crouzon syndrome Muenke syndrome Pfeiffer...
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Loeys–Dietz syndrome. Hypertelorism can also be seen in Apert syndrome, Autism spectrum disorder, craniofrontonasal dysplasia, Noonan syndrome, neurofibromatosis...
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syndrome Aortocaval compression syndrome Apert syndrome Apparent mineralocorticoid excess syndrome Arakawa's syndrome II Ardalan–Shoja–Kiuru syndrome...
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Acrocephalosyndactyly (ACS): type I – Apert syndrome type II – Crouzon syndrome type III – Saethre–Chotzen syndrome Robinow-Sorauf syndrome suggested to be included...
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a genetic basis.[citation needed] Apert syndrome Treacher Collins syndrome Hearing loss with craniofacial syndromes synd/1383 at Who Named It? L. E. O...
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Macrocephaly (redirect from Learman syndrome)
syndromes associated with macrocephaly that are noted in Signs and Symptoms of Genetic Conditions: A Handbook. Acrocallosal syndrome Apert syndrome...
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nonsyndromic cleft patients (Peterson-Falzone et al., 2001). Patients with Apert syndrome have a high occurrence of middle ear disease, otitis media and conductive...
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sickle cell disease, pseudohyperparathyroidism, Turner's syndrome, Down's syndrome, Apert syndrome, athyroidism, or osteodystrophy. It most frequently involves...
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like: Down syndrome Hydrocephalus Intrauterine growth restriction (IUGR) Premature birth Rarer causes include: Achondroplasia Apert syndrome Cleidocranial...
11 KB (1,227 words) - 03:46, 23 December 2023