Diastrophic dysplasia
| Diastrophic dysplasia | |
|---|---|
| Classification and external resources | |
| ICD-10 | Q77.5 |
| OMIM | 222600 |
| DiseasesDB | 30759 |
| eMedicine | orthoped/632 |
| Orphanet | 628 |
Diastrophic dysplasia (DTD) is an autosomal recessive[1] dysplasia which affects cartilage and bone development. ("Diastrophism" is a general word referring to a twisting.)[2] Diastrophic dysplasia is due to mutations in the SLC26A2 gene.
Affected individuals have short stature with very short arms and legs and joint problems that restrict mobility.
Symptoms
This condition is also characterized by an unusual clubfoot with twisting of the metatarsals, inward- and upward-turning foot, tarsus varus, and inversion adducted appearances. Furthermore, they classically present with scoliosis (progressive curvature of the spine), and unusually positioned thumbs (hitchhiker thumbs). About half of infants with diastrophic dysplasia are born with an opening in the roof of the mouth called a cleft palate. Swelling of the external ears is also common in newborns and can lead to thickened, deformed ears.
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.
Genetic prevalence
Diastrophic dysplasia affects about 1 in 100,000 births. It is one of a spectrum of skeletal disorders caused by mutations in the SLC26A2 gene. The protein encoded by this gene is essential for the normal development of cartilage and for its conversion to bone. Cartilage is a tough, flexible tissue that makes up much of the skeleton during early development. Most cartilage is later converted to bone, but in adulthood this tissue continues to cover and protect the ends of bones and is present in the nose and external ears. Mutations in the SLC26A2 gene alter the structure of developing cartilage, preventing bones from forming properly and resulting in the skeletal problems characteristic of diastrophic dysplasia.
This condition is an autosomal recessive disorder, meaning that the defective gene is located on an autosome, and both parents must carry one copy of the defective gene in order to have a child born with the disorder. The parents of a child with an autosomal recessive disorder are usually not affected by the disorder.
See also
Matt Roloff, a businessman and motivational speaker, has diastrophic dysplasia dwarfism. He is a vocal proponent of research and understanding of the disorder, as well as the assimilation of people with this disability into everyday life. The Little People of America is an organization of people with all kinds of short-stature syndromes, family members and caregivers, dedicated to improving the quality of life of affected persons, and improving their integration into society.
See also
External links
This article incorporates some public domain text from The U.S. National Library of Medicine
References
- ↑ Hästbacka J, Sistonen P, Kaitila I, Weiffenbach B, Kidd KK, De La Chapelle A (December 1991). "A linkage map spanning the locus for diastrophic dysplasia (DTD)". Genomics. 11 (4): 968–973. doi:10.1016/0888-7543(91)90021-6. PMID 1783404.
- ↑ "diastrophic - Definition from the Merriam-Webster Online Dictionary". Retrieved 2009-03-12.