e-ISSN: 2664-1194     print ISSN: 2304-6554
Apert syndrome ( Acrocephalosyndactyly)
Azerbaijan Journal of Perinatology and Pediatrics

Abstract

Apert syndrome is the most frequent reason of craniofacial deformation in newborn babies. This rare disease is characterized by premature fusion of some of the sutures of the skull and malformation of hands and feet. This article presents the clinical picture, diagnostic methods, principles of treatment and clinical case of newborn patient with Apert syndrome.

References

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Letra A, de Almeida AL, Kaizer R, Esper LA, Sgarbosa S. Intraoral features of Apert’s syndrome. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2007;103.

Surman TL, Logan RM, Townsend GC, Anderson PJ. Oral features in Apert syndrome: histological investigation. Orthod Craniofac Res 2010;13:61-7.

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Albuquerque MAP, Cavalcanti MGP. Computed tomography assessment of Apert syndrome. Braz Oral Res 2004;18:35-9.

Verma S, Draznin M. Apert syndrome. Dermatol Online J 2005;11:15.8.

PDF (Русский)
PDF (Русский)

Keywords

Apert syndrome
cranisynostosis
syndactyly Apert sindromu
kraniosinostoz
sindaktiliya синдром Аперта
краниосиностоз
синдактилия

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