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Biallelic CSGALNACT1-mutations cause a mild skeletal dysplasia
R Meyer1, S Schacht2, L Buschmann1
1Institute of Human Genetics, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Bone
|July 21, 2019
Summary
Genetic mutations in CSGALNACT1 cause mild skeletal dysplasia and joint laxity. This study identifies a new juvenile case, confirming the gene
Area of Science:
- Genetics
- Biochemistry
- Orthopedics
Background:
- Skeletal disorders often stem from genetic defects in bone and connective tissue synthesis.
- Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (CSGALNACT1) is crucial for glycosaminoglycan biosynthesis.
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