Diastrophic dysplasia, also referred to as disastrophic dwarfism, is a rare disorder that is congenital. The disorder is often characterized by short stature and unusually short arms and legs, abnormal development of bones and joints, progressive abnormal curvature of the spine, abnormal tissue changes of the outer and malformations of the head and facial (craniofacial) area.
Diastrophic dysplasia is caused by mutations in the SLC26A2 gene. It is the gene that provides instructions for making a protein that is essential for the normal development of cartilage and for its conversion to bone. The mutation in the SLC26A2 gene alters the structure of developing cartilage, preventing bones from forming properly and resulting in the skeletal problems.
Those with the genetic disorder have short stature with very short arms and legs. Most of the cases also have early-onset joint pain (osteoarthritis) and joint deformities called contractures that restrict movement. These complications can make it difficult for one to walk, and it worsens with age.
Diastrophic dysplasia is also linked to inward and downward-turning foot (a clubfoot), progressive abnormal curvature of the spine and unusually positioned thumbs. Swelling of the external ears is also common which might lead to deformed ears.
Another skeletal disorder called atelosteogenesis type 2 has similar signs and the disorder is often confused with that. Diastrophic dysplasia is less severe than atelosteogenesis type 2, though affected infants can also have breathing problems apart from skeletal problems.
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The signs and symptoms of diastrophic dysplasia are similar to those of another skeletal disorder called atelosteogenesis type 2; however, diastrophic dysplasia tends to be less severe.read more
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