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Τι (ποιος) είναι iron storage disease - ορισμός
ENDOCRINE DISEASE
Glycoprotein storage disease; Glycoprotein storage diseases
Glycogen storage disease type I
RARE DISEASE
Von Gierke's Disease; Von Gierke disease; Glucose-6-phosphatase deficiency; Von Gierke's disease; GSD type I; Glycogen storage disease type 1B; Glycogen storage disease type i; Gierke's disease; Von Gierke Disease; GSD I; Hepato-renal glycogenesis; Glerke's disease; Glycogen storage disease type 1b; Glycogen storage disease type 1C; Type 1 glycogen storage disease; Von gierke; Von gierke disease; Von Gierke's syndrome
Glycogen storage disease type I (GSD I) is an inherited disease that results in the liver being unable to properly break down stored glycogen. This impairment disrupts the liver's ability to break down stored glycogen that is necessary to maintain adequate blood sugar levels.
Lysosomal storage disease
INHERITED METABOLIC DISORDER THAT INVOLVE AN ABNORMAL ACCUMULATION OF SUBSTANCES INSIDE THE LYSOSOME RESULTING FROM DEFECTS IN LYSOSOMAL FUNCTION
Lysosomal storage disorder; Lysosomal storage diseases; Lysosomal storage diseases, nervous system; Lysosomal disorders; Lysosomal storage disorders; Lysosomal Storage Disease; Lysosomal disorder; Lysosomal disease
Lysosomal storage diseases (LSDs; ) are a group of over 70 rare inherited metabolic disorders that result from defects in lysosomal function. Lysosomes are sacs of enzymes within cells that digest large molecules and pass the fragments on to other parts of the cell for recycling.
lipidosis
LYSOSOMAL STORAGE DISEASE THAT INVOLVES THE ACCUMULATION OF HARMFUL AMOUNTS OF LIPIDS (FATS) IN SOME OF THE BODY'S CELLS AND TISSUES ME GUSTA LA VERGA
Lipid storage disease; Lipid storage; Lipid storage disorders; Lipid Storage Disease; Lipidoses; Lipid metabolism, inborn errors; Lipoidosis; Lipidosis; Lipid storage diseases
[?l?p?'d??s?s]
(also lipoidosis)
¦ noun (plural lipidoses -si:z) Medicine a disorder of lipid metabolism in the tissues.
Βικιπαίδεια
Glycoproteinosis
Glycoproteinosis are lysosomal storage diseases affecting glycoproteins, resulting from defects in lysosomal function. The term is sometimes reserved for conditions involving degradation of glycoproteins.
