The spectrum of Apert syndrome: phenotype, particularities in orthodontic treatment, and characteristics of orthognathic surgery

Author:

Hohoff Ariane,Joos Ulrich,Meyer Ulrich,Ehmer Ulrike,Stamm Thomas

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),General Dentistry,Otorhinolaryngology

Reference35 articles.

1. Cohen MM: Apert syndrome, not Apert's syndrome: Apert neither had nor owned the syndrome that bears his name. Plast Reconstr Surg. 1997, 100: 532-533.

2. Wheaton SW: Two specimens of congenital cranial deformity in infants associated with fusion of fingers and toes. Trans Pathol Soc Lond. 1894, 45: 238-241.

3. Tolarova MM, Harris JA, Ordway DE, Vargervik K: Birth prevalence, mutation rate, sex ratio, parents' age, and ethnicity in Apert syndrome. Am J Med Genet. 1997, 72: 394-398. 10.1002/(SICI)1096-8628(19971112)72:4<394::AID-AJMG4>3.0.CO;2-R.

4. Arroyo Carrera I, Martinez-Frias ML, Marco Perez JJ, Paisan Grisolia L, Cardenes Rodriguez A, Nieto Conde C, Felix Rodriguez V, Egues Jimeno JJ, Morales Fernandez MC, Gomez-Ullate Vergara J, Pardo Romero M, Penas Valiente A, Olivan del Cacho MJ, Lara Palma A: Apert syndrome: clinico-epidemiological analysis of a series of consecutive cases in Spain. An Esp Pediatr. 1999, 51: 667-672.

5. Ibrahimi OA, Chiu ES, McCarthy JG, Mohammadi M: Understanding the molecular basis of Apert syndrome. Plast Reconstr Surg. 2005, 115: 264-270.

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