There may be a relatively increased prevalence in Finland ref.
Typically there is limb shortening, hitchhiker thumbs, spinal deformity, and large joint contractures with associated deformities and premature degenerative disease. Other classic findings include ulnar deviation of the fingers, a large sandal gap (space between first and second pedal digits), and clubfoot. IQ is usually normal 6.
Larger than normal collagen fibrils have been extracted from the cartilage matrix in these patients.
It carries an autosomal recessive inheritance and thought to be due to mutations in the diastrophic dysplasia sulfate transporter (SLC26A2) gene located at chromosome 5q32-q33.1, resulting in under-sulfated proteoglycans in the cartilage matrix.
The bones are characterised by crescent-shaped flattened epiphyses, a short, broad femoral neck, and shortening and metaphyseal widening of the tubular bones. There is irregular deformity and shortening of the metacarpal bones, metatarsal bones, and phalanges. Abduction of the great toes and clubfeet may also be observed.
Treatment and prognosis
Life expectancy and mental function are usually normal. In view of its autosomal recessive inheritance, there is a 25% change of recurrence. Orthopaedic input and intervention is often required for correction or stabilisation of skeletal deformities.
History and etymology
The term diastrophic implies twisting and describes the twisted habitus in diastrophic dysplasia.
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