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what mutation(passive) is caused bya _ _ _ _ _ storage disease glycogen McArdle 's
by deficiency(passive) caused bySevere glycogen storage disease
by a deficiency in liver glycogen phosphorylase or other components of the associated phosphorylase cascade system.[1(passive) caused bya type of glycogen storage disease
by a deficiency in liver glycogen phosphorylase or other components of the associated phosphorylase cascade system(passive) caused bya type of glycogen storage disease
a deficiency in liver glycogen phosphorylase or other components of the associated phosphorylase cascade system(passive) caused bya type of glycogen storage disease
by a deficiency in liver glycogen phosphorylase or other components of(passive) caused bya type of glycogen storage disease
GM wheatmay causeGlycogen Storage Disease IV ... resulting in
by deficiency of acid alpha - glucosidase ( GAA(passive) caused bya lysosomal glycogen storage disease
by mutations(passive) caused byglycogen storage disease IV
What lipid storage disease ... by a deficiency of the enzyme glucocerebrosidase(passive) is causedlipid storage disease
genetically modified wheatmay causeGlycogen Storage Disease IV
the deficiency of a single hydrolase ( lysosomal enzymes(passive) is caused byLysosomal storage disease
by deficiency of the enzyme acid alpha - glucosidase(passive) caused byglycogen storage disease
by mutations in the same glycogen - branching enzyme gene(passive) caused byglycogen storage disease
by a deficiency of the lysosomal enzyme(passive) caused bya glycogen storage disease
a deficiency of enzymes that are require to perform metabolic functions(passive) is caused byLysosomal storage disease
a gene change , or mutation(passive) is caused byGlycogen Storage Disease
Deficiency of this enzymeleadsto glycogen storage disease
by a deficiency in liver glycogen phosphorylase or other components of the associated phosphorylase cascade system.[1(passive) caused byglycogen storage disease
by a deficiency in liver glycogen phosphorylase or other components of the associated phosphorylase cascade system.[2(passive) caused byglycogen storage disease
by a deficiency of acid alpha - glucosidase ( GAA(passive) caused bya glycogen storage disease
by a deficiency in acid(passive) caused bya glycogen storage disease
whose genetic inactivationcauseslysosomal storage disease
by a deficiency in liver glycogen phosphorylase or other components of the associated phosphorylase cascade system(passive) caused byglycogen storage disease
by a deficiency in liver glycogen phosphorylase or other components of the associated(passive) caused byglycogen storage disease
by a deficiency in liver glycogen phosphorylase or other components of the associated phosphorylase(passive) caused byglycogen storage disease
an inherited deficiency of the branching enzymecausesglycogen - storage disease
by deficiency of the glycogen(passive) caused byglycogen storage disease
by a deficiency of lysosomal a - glucosidase(passive) caused byA glycogen storage disease
by a deficiency of glucose(passive) is causeda glycogen storage disease
The Thr83Met mutationcausesglycogen storage disease XV
by a deficiency(passive) caused byglycogen storage disease
deficiencycausesglycogen storage disease
by mutations(passive) caused byglycogen storage disease
by a deficiency in liver glycogen phosphorylase or other components of the(passive) caused byglycogen storage disease
by a deficiency in liver glycogen phosphorylase or other(passive) caused byglycogen storage disease
by a deficiency in liver glycogen phosphorylase(passive) caused byglycogen storage disease
by a deficiency in liver glycogen phosphorylase or other components of the associated phosphorylase cascade(passive) caused byglycogen storage disease
by deficiency of the glycogen debranching enzyme(passive) caused byglycogen storage disease
by a deficiency of liver phosphorylase(passive) caused byA glycogen storage disease
in storage of extra glycogen in the liverdoes ... resultin storage of extra glycogen in the liver
in storage of extra glycogen in the liverresultin storage of extra glycogen in the liver
to exercise intoleranceleadsto exercise intolerance
uric acidto causeuric acid
1results1
cirrhosiscausescirrhosis
to damage to the liver over timeleadsto damage to the liver over time
in enlarged liver , cirrhosis of the liver and failure to thriveresultsin enlarged liver , cirrhosis of the liver and failure to thrive
Each lipid storage disorder results from deficiency of a specific enzymatic activitycausesEach lipid storage disorder results from deficiency of a specific enzymatic activity
in an abnormal metabolism of lipidsresultsin an abnormal metabolism of lipids
from deficiency of the enzyme acidresultedfrom deficiency of the enzyme acid
to abnormal bleeding and thrombosismay leadto abnormal bleeding and thrombosis
The cause of glycogen storage disease is geneticCausesThe cause of glycogen storage disease is genetic
through a deficiency incausedthrough a deficiency in
from the deficiency of resultsfrom the deficiency of
accumulation of glycogen on cardiac tissuescausesaccumulation of glycogen on cardiac tissues
in accumulation of lysosomes throughout the bodyresultingin accumulation of lysosomes throughout the body
from a defect in an enzyme required for either synthesis or degradationResultfrom a defect in an enzyme required for either synthesis or degradation
due to mutation or lack of functional genecauseddue to mutation or lack of functional gene
progressive limb girdle myopathy with diaphragmatic and cardiac muscle involvementcausesprogressive limb girdle myopathy with diaphragmatic and cardiac muscle involvement
excessive glycogen buildupcausesexcessive glycogen buildup
to progressive muscle weaknessleadsto progressive muscle weakness
to heart failuremay eventually leadto heart failure
to neurological disordersleadsto neurological disorders
to neurodegeneration and neurological deficitsleadsto neurodegeneration and neurological deficits
to exercise intoleranceleadsto exercise intolerance
Cardiac hypertrophy(passive) caused byCardiac hypertrophy
problems in different parts of the body , including the liver , muscles , kidneys , and heartcan causeproblems in different parts of the body , including the liver , muscles , kidneys , and heart
from a deficiency of the enzyme alpha - D - mannosidase in various organresultingfrom a deficiency of the enzyme alpha - D - mannosidase in various organ
from a defect in glycoprotein metabolismresultsfrom a defect in glycoprotein metabolism
her to have low blood sugarcausesher to have low blood sugar
to myopathieswill leadto myopathies
increased glycogen deposits in liver tissue , which follows inflammation and scarringcausesincreased glycogen deposits in liver tissue , which follows inflammation and scarring
in cell damage and organ dysfunctionresultsin cell damage and organ dysfunction
from a deficiency of the enzyme alpha - D - mannosidase in various organs , including brain , kidney andresultingfrom a deficiency of the enzyme alpha - D - mannosidase in various organs , including brain , kidney and
from a deficiency of the enzyme alpha - D - mannosidase in various organs , including brain , kidneyresultingfrom a deficiency of the enzyme alpha - D - mannosidase in various organs , including brain , kidney
varied symptoms involving different systems in the bodycausesvaried symptoms involving different systems in the body
in a proliferation of sulfatideresultingin a proliferation of sulfatide
from a deficiency of the enzyme alpha galactosidase ( GLA ) , which causes a glycolipid known as globotriaosylceramide to accumulate in blood vessels and other tissuesresultsfrom a deficiency of the enzyme alpha galactosidase ( GLA ) , which causes a glycolipid known as globotriaosylceramide to accumulate in blood vessels and other tissues
from defects in glycogen metabolismresultingfrom defects in glycogen metabolism