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A novel sequence variant in SFRP4 causing Pyle disease
Chelna Galada1, Hitesh Shah2, Anju Shukla1
1Department of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, India.
Pyle disease (PYL) is a rare bone disorder. A novel mutation in the SFRP4 gene was identified in a patient, confirming its role in PYL development.
Area of Science:
- Genetics
- Orthopedics
- Rare Diseases
Background:
- Pyle disease (PYL) is an extremely rare skeletal dysplasia characterized by irregular long bone development.
- Recent research identified homozygous mutations in the secreted frizzled-related protein 4 (SFRP4) gene as causative for PYL.
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