A rare manifestation of Fabry's disease
Swiss Med Wkly
.
2007 Feb 24;137(7-8):130.
doi: 10.4414/smw.2007.11649.
Authors
Zsanett Fricska Nagy
,
Krisztina Bencsik
,
Cecilia Rajda
,
Márta Morvay
,
Sándor Husz
,
Erika Vörös
,
Arndt Rolfs
,
Viktor Honti
,
Attila Dobozy
,
László Vécsei
PMID:
17370152
DOI:
10.4414/smw.2007.11649
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Adult
Amino Acid Substitution / genetics
Fabry Disease / genetics
Fabry Disease / pathology*
Humans
Male
Paresis / genetics
Paresis / pathology*
Stroke / genetics
Stroke / pathology*
alpha-Galactosidase / genetics
Substances
alpha-Galactosidase