Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. It is classified...

Shprintzen-Goldberg syndrome: craniosynostosis with marfanoid habitus and tissue anomalies. Apert syndrome Carpenter syndrome Crouzon syndrome Muenke syndrome Pfeiffer...

Loeys–Dietz syndrome. Hypertelorism can also be seen in Apert syndrome, Autism spectrum disorder, craniofrontonasal dysplasia, Noonan syndrome, neurofibromatosis...

syndrome Aortocaval compression syndrome Apert syndrome Apparent mineralocorticoid excess syndrome Arakawa's syndrome II Ardalan–Shoja–Kiuru syndrome...

nonsyndromic cleft patients (Peterson-Falzone et al., 2001). Patients with Apert syndrome have a high occurrence of middle ear disease, otitis media and conductive...

syndromes associated with macrocephaly that are noted in Signs and Symptoms of Genetic Conditions: A Handbook. Acrocallosal syndrome Apert syndrome...

a genetic basis.[citation needed] Apert syndrome Treacher Collins syndrome Hearing loss with craniofacial syndromes synd/1383 at Who Named It? L. E. O...

Acrocephalosyndactyly (ACS): type I – Apert syndrome type II – Crouzon syndrome type III – Saethre–Chotzen syndrome Robinow-Sorauf syndrome suggested to be included...

sickle cell disease, pseudohyperparathyroidism, Turner's syndrome, Down's syndrome, Apert syndrome, athyroidism, or osteodystrophy. It most frequently involves...

Amniotic band syndrome Apert syndrome Autosomal recessive Robinow syndrome Basel–Vanagaite–Sirota syndrome (Microlissencephaly-Micromelia syndrome) Campomelic...