Article
Type 1 Gaucher disease: phenotypic expression and natural history in Japanese patients.
Blood cells, molecules & diseases - 1 Mar 1998
Ida H, Rennert O M, Ito T, Maekawa K, Eto Y
Abstract excerpt
Gaucher disease is caused by a deficiency of glucocerebrosidase, resulting in hepatosplenomegaly, pancytopenia, growth retardation and skeletal involvement. We analyzed data on genotype and key clinical parameters in 35 Japanese patients with Gaucher disease type 1. Our data demonstrated that ove...
Topics
- Adult
- Age of Onset
- Asian People
- Child
- Child, Preschool
- Female
- Gaucher Disease
- Genotype
- Humans
- Infant
- Japan
- Male
- Phenotype
- Retrospective Studies
- White People
