Multiple Microcrystal Deposition Within a Family
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Abstract
A family is described in which four members in three generations showed evidence of crystal deposition disease: two developed calcium pyrophosphate dihydrate (CPPD) crystal deposition, one calcific periarthritis, and one mixed crystal deposition disease (gout + chondrocalcinosis). This previously undescribed observation supports a possible role for nonspecific heritable connective tissue factors in predisposing to crystal deposition.
References
1.
McCarty Jr D, Hogan J, Gatter R, Grossman M
. Studies on pathological calcifications in human cartilage. I. Prevalence and types of crystal deposits in the menisci of two hundred fifteen cadavera. J Bone Joint Surg Am. 1966; 48(2):309-25.
View
2.
Zitnan D, Sitaj S
. Chondrocalcinosis articularis Section L Clinical and radiological study. Ann Rheum Dis. 1963; 22:142-52.
PMC: 1007340.
DOI: 10.1136/ard.22.3.142.
View
3.
Bjelle A
. Morphological study of articular cartilage in pyrophosphate arthropathy. (Chondrocalcinosis articularis or calcium pyrophosphate dihydrate crystal deposition diseases). Ann Rheum Dis. 1972; 31(6):449-56.
PMC: 1005975.
DOI: 10.1136/ard.31.6.449.
View
4.
FESSEL W, SIEGELAUB A, Johnson E
. Correlates and consequences of asymptomatic hyperuricemia. Arch Intern Med. 1973; 132(1):44-54.
View
5.
Utsinger P, Zvaifler N, Resnick D
. Calcium pyrophosphate dihydrate deposition disease without chondrocalcinosis. J Rheumatol. 1975; 2(3):258-64.
View