1  Marfan syndrome and congenital contractural arachnodactyly.

2  were diagnosed with congenital contractural arachnodactyly according to an established clinical scor

3 se, small mouth, micrognathia, cleft palate, arachnodactyly and intellectual disability.

4                      Congenital contractural arachnodactyly (CCA) is an autosomal dominant disorder t

5                      Congenital contractural arachnodactyly (CCA) is an autosomal dominant disorder t

6  studies have linked congenital contractural arachnodactyly (CCA), a usually mild heritable connectiv

7 n syndrome (MFS) and congenital contractural arachnodactyly (CCA), respectively, has highlighted thei

8 me (fibrillin-1) and congenital contractural arachnodactyly (fibrillin-2).

9  Marfan syndrome and congenital contractural arachnodactyly implicate fibrillins in the function and

10 other exhibited a classic CCA phenotype with arachnodactyly, joint contractures, and abnormal pinnae,

11 ssue disorder characterized by tall stature, arachnodactyly, lens subluxation, and a high risk of aor

12  Marfan syndrome and congenital contractural arachnodactyly, respectively.

13 etal manifestations (congenital contractural arachnodactyly score, 5.6+/-5.1 versus 9.8+/-3.6; P=0.01

14 ical presentation of congenital contractural arachnodactyly than pathogenic variants in the FBN2 cent

15 issue disorder named congenital contractural arachnodactyly, which presents with obligatory skeletal