PRIAPISM AND FABRY DISEASE - A CASE-REPORT

被引:7
|
作者
GARCIACONSUEGRA, J
PADRON, M
JAUREGUIZAR, E
CARRASCOSA, C
RAMOS, J
机构
[1] HOSP INFANTIL LA PAZ,DEPT PATHOL,E-28046 MADRID,SPAIN
[2] HOSP INFANTIL LA PAZ,DEPT PAEDIAT SURG,E-28046 MADRID,SPAIN
关键词
Alpha-galactosidase A deficiency; Cutaneous angiokeratomas; Fabry disease; Priapism;
D O I
10.1007/BF01959404
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
A 10-year-old boy presented with priapism of 10h duration which after unsuccessful conservative measures, was relieved by a saphenocorporeal shunt. A4-year history of intermittent vague aching of fingers and toes accompanied by lowgrade fever was reported. Fabry disease was confirmed by the lack α-galactosidase acitivity in serum and leucocytes. Other characteristic features of Fabry disease were not present. The condition was also diagnosed in his 14-year-old brother and suspected in his maternal grandfather who died at the age of 49 from renal failure of unknown aetiology. © 1990 Springer-Verlag.
引用
收藏
页码:500 / 501
页数:2
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