Ontology highlight
ABSTRACT:
SUBMITTER: Rafi MA
PROVIDER: S-EPMC4817953 | biostudies-other | 2015 Nov
REPOSITORIES: biostudies-other
Rafi Mohammad A MA Rao Han Zhi HZ Luzi Paola P Wenger David A DA
Molecular therapy : the journal of the American Society of Gene Therapy 20150902 11
Krabbe disease is an autosomal recessive disorder resulting from defects in the lysosomal enzyme galactocerebrosidase (GALC). GALC deficiency leads to severe neurological features. The only treatment for presymptomatic infantile patients and later-onset patients is hematopoietic stem cell transplantation (HSCT). This treatment is less than ideal with most patients eventually developing problems with gait and expressive language. Several naturally occurring animal models are available, including ...[more]