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Gaucher disease: Enzyme therapy in the acute neuronopathic variant

โœ Scribed by Prows, Cynthia A.; Sanchez, Nelson; Daugherty, Cynthia; Grabowski, Gregory A.


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
23 KB
Volume
71
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(19970711)71:1<16::aid-ajmg3>3.0.co;2-o

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โœฆ Synopsis


The responses to regular intravenous enzyme infusions were compared in two sibs with Gaucher disease type 2, the acute neuronopathic variant. Enzyme administration was begun at 7 months in patient 1 who had severe progressive visceral and neuronopathic disease. No significant effect of enzyme infusions was noted. Death occurred at 9 months. Patient 2 was prenatally diagnosed and enzyme infusions were initiated at age 4 days. Overall development progressed at a rate similar to her unaffected full sib until her death at 15.1 months. Slowly progressive esotropia, ocular paresis and dysphagia began at 8 months as did infiltrative pulmonary disease. Comparison of these clinical courses show significant visceral and neurologic effects of anticipatory enzyme therapy, but with unaltered outcome, for Gaucher disease type 2. Am.


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