Disease name

Spondylometaphyseal dysplasia, Kozlowski type
 Spondylometaphyseal dysplasia, Kozlowski type

Marker gene

Gene symbol Chromosome location Protein name
TRPV4 12q24.11 Transient receptor potential cation channel subfamily V member 4

Inheritance

상염색체 우성

MIM number

184252

Summary

Spondylometaphyseal dysplasia, Kozlowski type is characterized by short stature (short-trunk dwarfism), scoliosis, metaphyseal abnormalities in the femur (prominent in the femoral neck and trochanteric area), coxa vara and generalized platyspondyly. Prevalence is estimated at less than one in one million people. Intelligence is usually normal. The syndrome is caused by a mutation in the TRPV4 gene (12q24.1) and is transmitted in an autosomal dominant manner.