| Literature DB >> 16151910 |
S Wendt1, C Whybra, C Kampmann, E Teichmann, M Beck.
Abstract
Fabry disease is an inherited lysosomal storage disease caused by deficiency of alpha-galactosidase A. Enzyme replacement therapy for this multisystem progressive disease has been available only since 2001. We here report the first known successful pregnancy of a female patient receiving such therapy.Entities:
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Year: 2005 PMID: 16151910 DOI: 10.1007/s10545-005-0018-9
Source DB: PubMed Journal: J Inherit Metab Dis ISSN: 0141-8955 Impact factor: 4.982