Hyperostosis: Difference between revisions
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{{Infobox_Disease | |||
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| DiseasesDB = 30719 | |||
| ICD10 = {{ICD10|M|85|8|m|80}} | |||
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| MedlinePlus = | |||
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| MeshID = D015576 | |||
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==Overview== | |||
'''Hyperostosis''' is an excessive growth of [[bone]]. It may lead to [[exostosis]]. It occurs in many [[musculoskeletal disorders]]. | |||
It is the thickening of the cortical bone. | |||
[[Hyperphosphatemia]]-hyperostosis syndrome (HHS) is a rare autosomal recessive metabolic disorder characterized by elevated serum phosphate levels and radiological evidence of cortical hyperostosis.<ref name=Frishberg>{{ cite journal |author=Frishberg Y, Topaz O, Bergman R, Behar D, Fisher D, Gordon D, Richard G, Sprecher E |title=Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders |journal=J Mol Med. |year=2005 |month=Jan |volume=83 |issue=1 |pages=33-8 |pmid=15599692 }}</ref> HHS is caused by mutations in GALNT3.<ref name=Ichikawa>{{ cite journal |author=Ichikawa S, Guigonis V, Imel EA, Courouble M, Heissat S, Henley JD, Sorenson AH, Petit B, Lienhardt A, Econs MJ |title=Novel GALNT3 mutations causing hyperostosis-hyperphosphatemia syndrome result in low intact fibroblast growth factor 23 concentrations |journal=J Clin Endocrinol Metab. |year=2007 |month=May |volume=92 |issue=5 |pages=1943-7 |pmid=17311862 }}</ref> | |||
===Causes=== | |||
===Drug Side Effect=== | |||
* [[Isotretinoin]] | |||
=References= | |||
{{reflist|2}} | |||
==See also== | |||
* [[Infantile cortical hyperostosis]] | |||
{{Osteochondropathy}} | |||
[[Category:Gross pathology]] | |||
[[Category:Surgery]] | |||
{{WikiDoc Help Menu}} | |||
{{WikiDoc Sources}} | |||
Latest revision as of 18:29, 8 June 2015
| Hyperostosis | |
| ICD-10 | M85.8 |
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| DiseasesDB | 30719 |
| MeSH | D015576 |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Hyperostosis is an excessive growth of bone. It may lead to exostosis. It occurs in many musculoskeletal disorders.
It is the thickening of the cortical bone.
Hyperphosphatemia-hyperostosis syndrome (HHS) is a rare autosomal recessive metabolic disorder characterized by elevated serum phosphate levels and radiological evidence of cortical hyperostosis.[1] HHS is caused by mutations in GALNT3.[2]
Causes
Drug Side Effect
References
- ↑ Frishberg Y, Topaz O, Bergman R, Behar D, Fisher D, Gordon D, Richard G, Sprecher E (2005). "Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders". J Mol Med. 83 (1): 33–8. PMID 15599692. Unknown parameter
|month=ignored (help) - ↑ Ichikawa S, Guigonis V, Imel EA, Courouble M, Heissat S, Henley JD, Sorenson AH, Petit B, Lienhardt A, Econs MJ (2007). "Novel GALNT3 mutations causing hyperostosis-hyperphosphatemia syndrome result in low intact fibroblast growth factor 23 concentrations". J Clin Endocrinol Metab. 92 (5): 1943–7. PMID 17311862. Unknown parameter
|month=ignored (help)