Add to ORKGWe describe a female infant with Apert syndrome (acrocephalosyndactyly, type I) and a frontonasal encephalocele with unremarkable family history. Key words: Apert syndrome, frontonasal encephalocele, new mutatio
Background: Apert syndrome is considered as one of the most common craniosynostosis syndromes with a...
Background: The present paper describes the general and oral manifestations in a 32-year-old man pre...
Apert Syndrome is a rare autosomal dominant disorder characterized by premature fusion of sutures of...
We describe a female infant with Apert syndrome (acrocephalosyndactyly, type I) and a frontonasal en...
Apert syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostos...
Apert's syndrome (acrocephalosyndactyly) is a developmental malformation characterized by craniosyno...
Apert syndrome (AS) is indeed a rare congenital disorder that falls under the category of acrocephal...
Apert's syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynost...
Apert syndrome is named for the French physician. Eugene Apert in 1906 described the syndrome acroce...
Defined as a rare type I acrocephalosyndactyly syndrome which is clinically characterized by dysmorp...
Apert’s syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynost...
Apert syndrome is a rare Type I acrocephalosyndactyly syndrome. It is a congenital disorder characte...
Apert syndrome is a congenital acrocephalosyndactyly syndrome. It is mainly presented by craniosynos...
A 2 1/2 months old female child born of consanguineous marriage, presented with dysmorphic features ...
A 2 1/2 months old female child born of consanguineous marriage, presented with dysmorphic features ...
Background: Apert syndrome is considered as one of the most common craniosynostosis syndromes with a...
Background: The present paper describes the general and oral manifestations in a 32-year-old man pre...
Apert Syndrome is a rare autosomal dominant disorder characterized by premature fusion of sutures of...
We describe a female infant with Apert syndrome (acrocephalosyndactyly, type I) and a frontonasal en...
Apert syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostos...
Apert's syndrome (acrocephalosyndactyly) is a developmental malformation characterized by craniosyno...
Apert syndrome (AS) is indeed a rare congenital disorder that falls under the category of acrocephal...
Apert's syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynost...
Apert syndrome is named for the French physician. Eugene Apert in 1906 described the syndrome acroce...
Defined as a rare type I acrocephalosyndactyly syndrome which is clinically characterized by dysmorp...
Apert’s syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynost...
Apert syndrome is a rare Type I acrocephalosyndactyly syndrome. It is a congenital disorder characte...
Apert syndrome is a congenital acrocephalosyndactyly syndrome. It is mainly presented by craniosynos...
A 2 1/2 months old female child born of consanguineous marriage, presented with dysmorphic features ...
A 2 1/2 months old female child born of consanguineous marriage, presented with dysmorphic features ...
Background: Apert syndrome is considered as one of the most common craniosynostosis syndromes with a...
Background: The present paper describes the general and oral manifestations in a 32-year-old man pre...
Apert Syndrome is a rare autosomal dominant disorder characterized by premature fusion of sutures of...