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| {{SI}}
| | #redirect:[[Winchester_syndrome]] |
| {{CMG}} {{AE}} {{RT}}
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| ==Overview==
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| Nodulosis-arthropathy-osteolysis syndrome is an osteolysis syndrome associated with [[matrix metalloproteinase-2 deficiency]] and mutations in the [[metalloproteinase-2 gene]]. It is characterized by carpal-tarsal destruction, subcutaneous nodules, and generalized [[osteoporosis]] and shows [[autosomal recessive]] inheritance.<ref name="pmid19653001">{{cite journal |author=Gok F, Crettol LM, Alanay Y, ''et al.'' |title=Clinical and radiographic findings in two brothers affected with a novel mutation in matrix metalloproteinase 2 gene |journal=Eur. J. Pediatr. |volume=169 |issue=3 |pages=363–7 |year=2010 |month=March |pmid=19653001 |doi=10.1007/s00431-009-1028-7 |url=}}</ref>
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| ==References==
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| {{reflist|2}}
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| [[category:Disease]]
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| [[Category:Genetics]] | |
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| [[Category:Rare diseases]]
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| {{WH}}
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| {{WS}}
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