Acampomelic campomelic dysplasia is a rare clinical variant of the more commonly encountered campomelic dysplasia (CMD1), characterized by absence of long bone curvature (acampomelia). We present a patient with acampomelic CMD1 with a de novo SOX9 missense mutation and report his clinical course to age one year, thereby contributing to genotype-phenotype correlation in CMD1. 2000
Campomelic dysplasia (MIM 114290) is a severe malformation syndrome frequently accompanied by male-t...
Campomelic dysplasia (CD) and its variant acampomelic campomelic dysplasia (ACD) are caused by SOX9 ...
BackgroundCampomelic dysplasia (CD) is a rare disorder that involves the skeletal and genital system...
Campomelic dysplasia is a skeletal dysplasia characterized by flat face, Pierre Robin sequence, shor...
Campomelic dysplasia (CD) is an autosomal, dominantly inherited, skeletal abnormality belonging to t...
Abstract Background: Campomelic dysplasia (CD) is a semilethal developmental disorder caused by muta...
Campomelic dysplasia (CD) is an autosomal, dominantly inherited, skeletal abnormality belonging to t...
Campomelic dysplasia (CD) is an autosomal, dominantly inherited, skeletal abnormality belonging to t...
Campomelic dysplasia (CD; OMIM #114290) is an autosomal dominant, frequently lethal dysplasia syndro...
Campomelic dysplasia (CD; OMIM #114290) is an autosomal dominant, frequently lethal dysplasia syndro...
Background: Campomelic dysplasia and acampomelic campomelic dysplasia (ACD) are allelic disorders du...
Background Campomelic dysplasia (CD) is a semilethal developmental disorder caused by mutations in a...
Campomelic dysplasia (CD) is an autosomal dominant skeletal malformation syndrome with features incl...
Abstract OBJECTIVES: Campomelic dysplasia is a rare congenital skeletal disorder characterized by b...
Campomelic dysplasia is an alteration of bone development which is manifested as an autosomal domin...
Campomelic dysplasia (MIM 114290) is a severe malformation syndrome frequently accompanied by male-t...
Campomelic dysplasia (CD) and its variant acampomelic campomelic dysplasia (ACD) are caused by SOX9 ...
BackgroundCampomelic dysplasia (CD) is a rare disorder that involves the skeletal and genital system...
Campomelic dysplasia is a skeletal dysplasia characterized by flat face, Pierre Robin sequence, shor...
Campomelic dysplasia (CD) is an autosomal, dominantly inherited, skeletal abnormality belonging to t...
Abstract Background: Campomelic dysplasia (CD) is a semilethal developmental disorder caused by muta...
Campomelic dysplasia (CD) is an autosomal, dominantly inherited, skeletal abnormality belonging to t...
Campomelic dysplasia (CD) is an autosomal, dominantly inherited, skeletal abnormality belonging to t...
Campomelic dysplasia (CD; OMIM #114290) is an autosomal dominant, frequently lethal dysplasia syndro...
Campomelic dysplasia (CD; OMIM #114290) is an autosomal dominant, frequently lethal dysplasia syndro...
Background: Campomelic dysplasia and acampomelic campomelic dysplasia (ACD) are allelic disorders du...
Background Campomelic dysplasia (CD) is a semilethal developmental disorder caused by mutations in a...
Campomelic dysplasia (CD) is an autosomal dominant skeletal malformation syndrome with features incl...
Abstract OBJECTIVES: Campomelic dysplasia is a rare congenital skeletal disorder characterized by b...
Campomelic dysplasia is an alteration of bone development which is manifested as an autosomal domin...
Campomelic dysplasia (MIM 114290) is a severe malformation syndrome frequently accompanied by male-t...
Campomelic dysplasia (CD) and its variant acampomelic campomelic dysplasia (ACD) are caused by SOX9 ...
BackgroundCampomelic dysplasia (CD) is a rare disorder that involves the skeletal and genital system...