Effect of discontinuing of laronidase in a patient with mucopolysaccharidosis type I

被引：27

作者：

Anbu, AT ^{[1
]}

Mercer, J ^{[1
]}

Wraith, JE ^{[1
]}

机构：

[1] Royal Manchester Childrens Hosp, Willink Biochem Genet Unit, Manchester M27 4HA, Lancs, England

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 2006年 / 29卷 / 01期

关键词：

D O I：

10.1007/s10545-006-0237-8

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

We present a patient on enzyme replacement therapy who showed rapid deterioration when laronidase was discontinued owing to pregnancy.

引用

页码：230 / 231

页数：2

共 3 条

[1] Pregnancies in Gaucher disease: A 5-year study [J].

Elstein, Y ;

Eisenberg, V ;

Granovsky-Grisaru, S ;

Rabinowitz, R ;

Samueloff, A ;

Zimran, A ;

Elstein, D .

AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2004, 190 (02) :435-441

[2] Enzyme-replacement therapy in mucopolysaccharidosis I. [J].

Kakkis, ED ;

Muenzer, J ;

Tiller, GE ;

Waber, L ;

Belmont, J ;

Passage, M ;

Izykowski, B ;

Phillips, J ;

Doroshow, R ;

Walot, I ;

Hoft, R ;

Yu, KT ;

Okazaki, S ;

Lewis, D ;

Lachman, R ;

Thompson, JN .

NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (03) :182-188

[3] Enzyme replacement therapy for mucopolysaccharidosis I:: A randomized, double-blinded, placebo-controlled, multinational study of recombinant human α-L-iduronidase (Laronidase) [J].

Wraith, JE ;

Clarke, LA ;

Beck, M ;

Kolodny, EH ;

Pastores, GM ;

Muenzer, J ;

Rapoport, DM ;

Berger, KI ;

Swiedler, SJ ;

Kakkis, ED ;

Braakman, T ;

Chadbourne, E ;

Walton-Bowen, K ;

Cox, GF .

JOURNAL OF PEDIATRICS, 2004, 144 (05) :581-588

← 1 →