Hallazgos clínicos y genéticos de dos casos con síndrome de Apert

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Authors

Francisco Cammarata‐Scalisi · University of the Andes

Elanur Yılmaz · Akdeniz University

Michele Callea · Bambino Gesù Children's Hospital

Andrea Avendaño · University of the Andes

Ercan Mıhçı · Akdeniz University Hospital

Özgül M. Alper · Akdeniz University

Abstract

Two cases of Apert syndrome are described. It is important to recognize this uncommon entity through clinical findings, highlight interdisciplinary medical evaluation, and provide timely genetic counseling for the family.

Topics & Keywords

Craniofacial Disorders and Treatments History of Medical Practice Cleft Lip and Palate Research

UN Sustainable Development Goals

Good health and well-being

Publication Details

Published in: Boletín Médico del Hospital Infantil de México

Volume 76, Issue 1, pp. 44-48

DOI: 10.24875/bmhim.18000053

Field-Weighted Citation Impact: 0.89