Krabbe disease (KD) (also known as globoid cell leukodystrophy or galactosylceramide lipidosis) is a rare and often fatal lysosomal storage disease that...

leukodystrophy (MLD), (2) Krabbe disease, (3) X-Linked adrenoleukodystrophy (ALD), (4) Canavan disease, and (5) Alexander disease. Each type of leukodystrophy...

Sturge–Weber syndrome Other names Sturge–Weber–Krabbe disease CT scan of Sturge-Weber syndrome Specialty Medical genetics ...

is causing buildup. Lysosomal storage diseases include: Sphingolipidoses Ceramidase Farber disease Krabbe disease Infantile onset Late onset Galactosialidosis...

JC virus), CADASIL (caused by abnormal NOTCH3 protein activity), and Krabbe disease (caused by a deficiency of the enzyme galactosylceramidase). Progressive...

actor Sphingolipidoses Lysosomal storage disease Niemann–Pick disease Fabry disease Tay–Sachs disease Krabbe disease Metachromatic leukodystrophy Medical...

extremities) b) Galactocerebroside (galactosylceramidase) accumulation – Krabbe disease. Jurevics, H; Hostettler, J; Muse, ED; Sammond, DW; Matsushima, GK;...

Knud Haraldsen Krabbe (3 March 1885 – 8 May 1961) was a Danish neurologist. In 1916, he first described what is now known as Krabbe disease. He was considered...

Werner Siemens, Albert Touraine Christensen–Krabbe disease – Erna Christensen, Knud Krabbe Christmas disease – Stephen Christmas Churg–Strauss syndrome...

members of this group are Niemann–Pick disease, Fabry disease, Krabbe disease, Gaucher disease, Tay–Sachs disease and metachromatic leukodystrophy. They...