Enzyme replacement therapy in an adolescent with Fabry disease

Eur J Pediatr. 2003 Jul;162(7-8):522-523. doi: 10.1007/s00431-003-1222-y. Epub 2003 May 6.

Authors

Sabine Illsinger¹, Thomas Luecke², Hendrik Langen², Anibh M Das²

Affiliations

¹ Department of Paediatrics, Medical School, Carl-Neuberg Strasse 1, 30623, Hannover, Germany. Illsinger.Sabine@mh-hannover.de.
² Department of Paediatrics, Medical School, Carl-Neuberg Strasse 1, 30623, Hannover, Germany.

PMID: 12733069
DOI: 10.1007/s00431-003-1222-y

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Adolescent
Fabry Disease / genetics
Fabry Disease / therapy*
Humans
Isoenzymes / therapeutic use
Male
Pedigree
alpha-Galactosidase / therapeutic use

Substances

Isoenzymes
alpha-Galactosidase