Nodulosis-arthropathy-osteolysis syndrome: Difference between revisions

Latest revision as of 13:20, 27 July 2012

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-{{SI}}
+#redirect:[[Winchester_syndrome]]
-{{CMG}} {{AE}} {{RT}}
-==Overview==
-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>
-==References==
-{{reflist|2}}
-[[category:Disease]]
-[[Category:Genetics]]
-[[Category:Rare diseases]]
-{{WH}}
-{{WS}}