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Gaucher disease is an inherited disorder that affects many of the body's organs and tissues. The...
Pathology of Gaucher disease MGM medical college, Navi Mumbai, india
Gaucher Disease
Gaucher's disease Hepatomegaly Splenomegaly
Lysosomal storage disease Lysosomal storage disease Micrograph of Gaucher disease, with cells that ...
Important lipid storage diseases
genetics
In this slide deck, explore new treatment advances for acid sphingomyelinase deficiency (ASMD) in ad...
Lipids
IMAGEN HEMATOLOGICA E INFECCION
Lysosomes are sub cellular organelles responsible for the physiologic turnover of cell constituents....
It is believed by many that the intraoral production of acids from carbohydrate, arising from incomp...
lysosomal storage diseases
Short overview of some genetic disorders
A lysosomal storage disease caused by acid sphingomyelinase deficiency (ASMD), which catalyzes the h...
Spleen : Anatomy; Physiology;Classification;Etiology;Stepwise approach; Assosiated features; Investi...
By Dr Piyush Ojha , DM Resident, GMC Kota under guidance of Prof. Dr Vijay Sardana (HOD,Neurology)
GLYCOLIPIDS- DEFINITION, SOURCE, STRUCTURAL ILLUSTRATION, PROPERTIES, SYNTHESIS, CLASSIFICATION, EXT...
lysosomal storage disorders- brief description.
Splenomegaly : Spleen weight of 400-500gm 750 – 1000gm : prominent below costal margin >1000g...
Definition: Many childhood conditions are caused by gene mutations that encode specific proteins. Th...
Neurometabolic
