Autosomal recessive inheritance

   sex-linked (or X-linked) recessive inheritance

   Classification of Lipid storage diseases

   Sphingolipidosis

   Gaucher disease:

   Niemann-Pick disease

   Fabry’s disease:

   The gangliosidosis

   Krabbe disease

   Farber’s disease

   Metachromatic leukodystrophy (MLD):

   Fucosidosis

   -Mucolipidosis

   Mucolipidosis type II (1-cell disease):

   Mucolipidosis type III (pseudo-hurler polydystrophy):

   Miscellaneous

   Multiple sulfatase deficiency

   cholesterol ester storage disease:

   Batten disease

   Wolman Disease

   Organomegaly :

   Skeletal abnormalities

   Pulmonary infiltration

   Dermatologic findings

   Painful crises

   Vascular disease

   Laboratory Diagnosis of Lipid storage diseases

   Methods for diagnosis of Lipid storage diseases

   Laboratory Diagnosis of Gaucher disease

   Laboratory Diagnosis of Niemann-Pick disease

   Laboratory Diagnosis of Fabry’s disease

   Laboratory Diagnosis of GM1 Ganglisidosis disease

   Laboratory Diagnosis of GM2 Ganglisidosis disease

   Laboratory Diagnosis of krabbe disease

   Laboratory Diagnosis of Farber Disease

   Laboratory Diagnosis of Metachromatic Leukodystrophy

   Laboratory Diagnosis of Fucosidosis

   Mucolipidosis

   Laboratory Diagnosis of Mucolipidosis type II (1-cell disease)

   Laboratory Diagnosis of Mucolipidosis type III (pseudohurler polydystrophy)

   Miscellaneous

   Laboratory Diagnosis of Multiple sulphatase deficiency

   Laboratory Diagnosis of Cholesterol ester storage

   Laboratory Diagnosis of Batten disease

   Laboratory Diagnosis of Wolman’s disease