Structured Summary
Abstract
An asymptomatic, autosomal dominant trait in which pea-sized sclerotic spots, prominent in the metaphyseal area, are accompanied by unique cutaneous lesions. These are yellowish papules or plaques with increased elastin content. (From Cecil Textbook of Medicine, 19th ed, pp1434-35)
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Synonyms
1 entry terms
- Osteopoikiloses
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Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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Indexing Annotation
a form of osteosclerosis
MeSH Record
History Note
91(64); was see under OSTEOSCLEROSIS 1970-90; was see under BONE DISEASES 1967-69
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References
- National Library of Medicine. Osteopoikilosis. Medical Subject Headings (MeSH). 2026. Unique ID D010023. http://id.nlm.nih.gov/mesh/2026/D010023
- Osteopoikilosis. In: Wikipedia. https://en.wikipedia.org/wiki/Osteopoikilosis
- Osteopoikilosis. In: Wikidata. https://www.wikidata.org/wiki/Q1477777