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PMID: 382486 Published · ppublish English Case Reports Journal Article

Attempt at enzyme replacement by organ transplantation: renal transplantation in Gaucher disease.

Transplantation proceedings ·Vol. 11 ·No. 2 ·1979-06-00 ·Pages 1218-9

Groth CG, Collste H, Dreborg S, Håkansson G, Lundgren G, Svennerholm L

Abstract

Following renal transplantation, hepatic glucocerebroside deposits in a child with Gaucher disease were reduced. This suggests that enzyme replacement had been achieved.

MeSH Terms
Cadaver Child Female Gaucher Disease/enzymology,surgery Glucosidases/metabolism Glucosylceramidase/metabolism Glucosylceramides/metabolism Humans Kidney Transplantation Liver/metabolism Male Transplantation, Homologous
Chemicals
Glucosylceramides Glucosidases Glucosylceramidase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Groth C G
Collste H
Dreborg S
Håkansson G
Lundgren G
Svennerholm L
Article Info
Journal
Transplantation proceedings
Abbr.
Transplant Proc
ISSN
0041-1345
Published
1979-06-00
Pages
1218-9
Language
English
Region
United States
NLM ID
0243532
Subset
IM
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