Add to ORKGA 2 1/2 months old female child born of consanguineous marriage, presented with dysmorphic features and hand and foot deformities. Examination revealed craniofacial and limb dysmorphism in the form of brachycephaly, sutural fusion, open anterior fontanelle, hyperteleorism, malar hypoplasia, high arched palate with cleft palate, low set ears and syndactyly in all digits of hands and feet (Figure 1). There were no other associated congenital anomalies. Based on clinico-radiological evaluation a diagnosis of Apert syndrome was made
Apert syndrome (AS) is a rare type of congenital craniofacial dysmorphic and severe syndactyly of th...
Apert syndrome is a rare Type I acrocephalosyndactyly syndrome. It is a congenital disorder characte...
Apert Syndrome is a rare autosomal dominant disorder characterized by premature fusion of sutures of...
A 2 1/2 months old female child born of consanguineous marriage, presented with dysmorphic features ...
Apert syndrome (AS) is indeed a rare congenital disorder that falls under the category of acrocephal...
Apert syndrome is a congenital acrocephalosyndactyly syndrome. It is mainly presented by craniosynos...
Apert syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostos...
Apert's syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynost...
Apert syndrome is a rare craniosynostosis syndrome characterized by irregular craniosynostosis, midf...
Apert syndrome was diagnosed in a newborn with typical facial and digital features whose only detect...
Defined as a rare type I acrocephalosyndactyly syndrome which is clinically characterized by dysmorp...
Apert syndrome is named for the French physician. Eugene Apert in 1906 described the syndrome acroce...
We describe a female infant with Apert syndrome (acrocephalosyndactyly, type I) and a frontonasal en...
Apert's syndrome (acrocephalosyndactyly) is a developmental malformation characterized by craniosyno...
We describe a female infant with Apert syndrome (acrocephalosyndactyly, type I) and a frontonasal en...
Apert syndrome (AS) is a rare type of congenital craniofacial dysmorphic and severe syndactyly of th...
Apert syndrome is a rare Type I acrocephalosyndactyly syndrome. It is a congenital disorder characte...
Apert Syndrome is a rare autosomal dominant disorder characterized by premature fusion of sutures of...
A 2 1/2 months old female child born of consanguineous marriage, presented with dysmorphic features ...
Apert syndrome (AS) is indeed a rare congenital disorder that falls under the category of acrocephal...
Apert syndrome is a congenital acrocephalosyndactyly syndrome. It is mainly presented by craniosynos...
Apert syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostos...
Apert's syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynost...
Apert syndrome is a rare craniosynostosis syndrome characterized by irregular craniosynostosis, midf...
Apert syndrome was diagnosed in a newborn with typical facial and digital features whose only detect...
Defined as a rare type I acrocephalosyndactyly syndrome which is clinically characterized by dysmorp...
Apert syndrome is named for the French physician. Eugene Apert in 1906 described the syndrome acroce...
We describe a female infant with Apert syndrome (acrocephalosyndactyly, type I) and a frontonasal en...
Apert's syndrome (acrocephalosyndactyly) is a developmental malformation characterized by craniosyno...
We describe a female infant with Apert syndrome (acrocephalosyndactyly, type I) and a frontonasal en...
Apert syndrome (AS) is a rare type of congenital craniofacial dysmorphic and severe syndactyly of th...
Apert syndrome is a rare Type I acrocephalosyndactyly syndrome. It is a congenital disorder characte...
Apert Syndrome is a rare autosomal dominant disorder characterized by premature fusion of sutures of...