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Sclerosteosis

Known as: SCLEROSTEOSIS 1, Cortical hyperostosis with syndactyly, SOST1 
National Institutes of Health

Related topics

Related topics

15 relations
Autosomal recessive inheritanceChronic HeadacheEsotropiaExophthalmos

Broader (2)

HyperostosisSyndactyly

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Accelerated development of instability-induced osteoarthritis in transgenic mice overexpressing SOST.
OBJECTIVE Sclerostin (SOST), acting as a Wnt antagonist, has been shown to play a key role in regulating bone homestasis, and has… 
2016
2016
Sclerosteosis caused by a novel nonsense mutation of SOST in a consanguineous family
Sclerosteosis, characterized by the hyperostosis of cranial and tubular bones, is a rare autosomal recessive hereditary disorder… 
2015
2015
A Novel Loss-of-Sclerostin Function Mutation in a First Egyptian Family with Sclerosteosis
Sclerosteosis is a rare autosomal recessive condition characterized by increased bone density. Mutations in SOST gene coding for… 
2015
2015
Sclerosteosis (craniotubular hyperostosis-syndactyly) with complex hyperphalangy of the index finger
We report a 4-year-old boy with sclerosteosis associated with severe digital dysostosis. The initial medical consultation was… 
2014
2014
Novel SOST gene mutation in a sclerosteosis patient from Morocco: a case report.
2013
2013
Management of trigeminal neuralgia in sclerosteosis
Background: Sclerosteosis is a rare bone disorder characterized by a progressive craniotubular hyperostosis. The diagnosis of… 
2013
2013
An Enhanced Particle Swarm Optimization for Design of Pin Connected Structures
2012
2012
Mechanical Properties of Bone Due to SOST Expression: A 3-Point Bending Assessment of Murine Femurs
Sclerostin, a protein coded for by the SOST gene, is an osteocyte-expressed negative regulator of bone formation. The absence of… 
2010
2010
A Forty Five Years Female Patient with Sclerosteosis
Sclerosteosis is a rare autosomal recessive disorder, characterized by progressive, generalized bony overgrowth of the calvarium… 
Review
2006
Review
2006
Wnt signaling is involved in the inhibitory action of sclerostin on BMP-stimulated bone formation.
357 Sclerosteosis and van Buchem disease are two rare, closely related skeletal disorders characterized by a substantial increase… 
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