New Zealand Lysosomal Storage Diseases support group
Learn more about:
Hurler syndrome
Mucolipidosis type II
Niemann-Pick Disease Type C
Mucopolysaccharidosis type VI
Mucopolysaccharidosis Type IVA
Pompe disease
Sly syndrome
Mucopolysaccharidosis type IV-B
Gaucher disease type 3
Gaucher disease type 2
Gaucher disease type I
Farber’s disease
Gangliosidosis GM1 type 3
Gangliosidosis- generalized GM1 type 2
Gangliosidosis generalized GM1- type 1
Niemann-Pick Disease Type D
Niemann-Pick Disease
Tay Sachs disease
Batten disease
Hunter Syndrome
Mucolipidosis type III
Mucolipidosis type 4
Mucopolysaccharidosis type I
Mucolipidosis type I
Krabbe disease
Wolman disease
LDNZ was set up in 1999 to fill a gap in information and support for families affected by Lysosomal Storage Diseases in New Zealand.