Spondyloepimetaphyseal dysplasia, Pakistani type

Spondyloepimetaphyseal dysplasia, Pakistani type is a form of spondyloepimetaphyseal dysplasia involving PAPSS2 (also known as "ATPSK2"). The condition is rare.

Genetics

This condition is inherited in an autosomal recessive fashion. It is due to mutations in the Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthetase 2 (PAPSS2) gene which is located on the long arm of chromosome 10 (10q23.2-q23.31).

Treatment

History

This condition was first described in a large eight generation consanguineous Pakistani family.

The causative mutation was identified in 1998.

References

External links

1. Spondyloepimetaphyseal dysplasia
2. Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
3. Osteogenesis imperfecta
4. Chromosome 10
5. PAPSS2
6. List of OMIM disorder codes