Sclérostéose
The sclérostéose is the most serious form of the change of the Gène SOST located on the locus q12-q21 of the Chromosome 17 coding the sclérostine. The other form is the Maladie of Van Buchem. This disease is also called hyperostose cortical syndactylie
- This disease is with recessive autosomic Transmission.
- For description supplements this disease to see the article Dysplasies osseous in connection with gene SOST
Sources
- Online Mendelian Inheritance in Man, OMIM (TM). Johns Hopkins University, Baltimore, MANDELEVIUM. MIM Number: 269500 * GeneTests: Medical Genetics Information Resource (database online). Copyright, University off Washington, Seattle. 1993-2005]
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