Medicine:Hyperostosis
From HandWiki
Hyperostosis is an excessive growth of bone. It may lead to exostosis. It occurs in many musculoskeletal disorders and from use of drugs like Isotretinoin.[1]
Disorders featuring hyperostosis include:[2]
- Camurati-Engelmann disease, type 2
- Hypertrophic osteoarthropathy, primary, autosomal recessive, 2
- Melorheostosis
- Tumoral calcinosis, hyperphosphatemic, familial, 1
- Worth disease
See also
- Diffuse idiopathic skeletal hyperostosis
- Hyperostosis frontalis interna
- Infantile cortical hyperostosis
- Porotic hyperostosis
- SAPHO syndrome
References
- ↑ Ellis, Charles N.; Pennes, David R.; Hermann, Richard C.; Blauvelt, Andrew; Martel, William; Voorhees, John J. (June 1988). "Long-term radiographic follow-up after isotretinoin therapy" (in en). Journal of the American Academy of Dermatology 18 (6): 1252–1261. doi:10.1016/S0190-9622(88)70131-0. https://linkinghub.elsevier.com/retrieve/pii/S0190962288701310.
- ↑ "Hyperostosis (Concept Id: C0020492)" (in en). https://www.ncbi.nlm.nih.gov/medgen/9366.
- Stuart-Macadam P (April 1985). "Porotic hyperostosis: representative of a childhood condition". American Journal of Physical Anthropology 66 (4): 391–8. doi:10.1002/ajpa.1330660407. PMID 3887936.
- "Infantile cortical hyperostosis". Archives of Disease in Childhood 90 (7): 711. July 2005. doi:10.1136/adc.2004.065334. PMID 15970613.
- "SAPHO syndrome: a long-term follow-up study of 120 cases". Seminars in Arthritis and Rheumatism 29 (3): 159–71. December 1999. doi:10.1016/S0049-0172(99)80027-4. PMID 10622680.
- "Hyperostosis frontalis interna; two contrasting cases". Journal of the American Medical Association 148 (3): 199–200. January 1952. doi:10.1001/jama.1952.62930030004009b. PMID 14880497.
External links
| Classification |
|---|
 |  |
