Esophageal atresia/Tracheoesophageal fistula Definition Congenital obstruction of the esophagus characterized by interrupted the continuity of the esophageal wall with one…

Limb Development Overview of Limb Formation Initiation of Limb Development Limb Field Limb Bud Outgrowth of the Limb Bud Apical Ectodermal Ridge (AER) Limb Bud Mesoderm Morphogenetic…

Syndrome spotter• Definition – “a collection of traits, health problems, and/or birth defects in an individual which usually has a single underlying cause”

A case report of Turner syndrome associated with fetal nuchal cystic hygroma and bilateral syndactyly of the hands and feetCASE REPORT Open Access A case report of Turner

Copyright 2018 by Korean Society for Surgery of the Hand, Korean Society for Microsurgery, and Korean Society for Surgery of the Peripheral Nerve. All Rights reserved. This

INTRODUCTION Pfeiffer syndrome (PS) is a rare autosomal dominant con- genital disorder, originally described by Pfeiffer in 1964, and is characterized by an acrocephalic

Pfeiffer syndrome type II discovered perinatally: Report of an observation and review of the literatureLETTER / Musculoskeletal imaging Pfeiffer syndrome type II discovered

Dilemmas on a Case with Craniosynostosis Diagnosed as Pfeiffer Syndrome by DNA AnalysisWorld Journal of Oral and Maxillofacial Surgery 2019 | Volume 2 | Issue 1 | Article

A Guide to the Diagnosis and Treatment of Apert SyndromeA Guide to the Diagnosis and Treatment of Apert Syndrome Having a child born with Apert syndrome may feel over- whelming.

Apert syndromeApert syndrome Description Apert syndrome is a genetic disorder characterized by skeletal abnormalities. A key feature of Apert syndrome is the premature closure