PRIMARY HYPEROXALURIA - A CASE-REPORT

被引：3

作者：

BRETT, F

KEALY, WF

MURNAGHAN, D

HOGAN, JM

机构：

[1] Departments of Histopathology, Regional Hospital, Wilton Cork

来源：

IRISH JOURNAL OF MEDICAL SCIENCE | 1990年 / 159卷 / 03期

关键词：

D O I：

10.1007/BF02946674

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

A case of primary hyperoxaluria which presented with progressive renal failure in a 34 year old woman is reported. The patient died six years following the initial diagnosis and post mortem examination revealed widespread deposition of oxalate crystals in her tissues. © 1990 Springer.

引用

页码：78 / 79

页数：2

共 5 条

[1]

Danpure C.J., Jennings P.R., Peroxisomal alanine gly oxalate aminotransferase deficiency in primary hyperoxaluria type I, FEBS Lett., 201, pp. 20-24, (1986)

[2]

Willia H.E., Smith L.H., Primary hyperoxaluria, The metabolicbasis of inherited disease, pp. 204-228, (1983)

[3]

Bourke E., Costello J., The clinical importance of oxalic acid, Journal of the Irish Medical Association, 68, pp. 93-96, (1975)

[4]

Toon C.R.V., Channon S.M., Parkinson I.S., Morley A.R., Lennard T.W.J., Parrott N.R., Laker M.F., Plasma oxalate concentration and secondary oxalosis in patients with chronic renal failure, J. Clin. Path, 41, pp. 1107-1113, (1988)

[5]

Oli H., Davidson A.M., Adult systemic oxalosis presenting as acute renal failure, Postgraduate Medical Journal, 55, pp. 44-45, (1979)

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