Deficiency of alpha-1,4-glucosidasemay causeGLYCOGEN STORAGE DISEASE TYPE II.Hexosaminidases
a deficiency of muscle phosphofructokinase and characterized by muscular weakness(passive) caused byPFKM A glycogen storage disease
a deficiency in liver glycogen phosphorylase or other components of the associated phosphorylase cascade system.[2(passive) caused byglycogen storage disease
PreventionThere ... no simple wayto preventglycogen storage disease
a deficiency of acid alpha - glucosidase ( GAA(passive) caused bya glycogen storage disease
genetic defects that results in deficiency in certain enzymes of glycogen metabolism(passive) are caused byGlycogen Storage diseases
the lack of an enzyme needed to change glucose into glycogen and break down glycogen into glucose(passive) are caused byGlycogen storage diseases
Mutations in the glucose-6-phosphatase genecauseglycogen storage disease 1a
other problems ... no wayto preventglycogen storage disease
a deficiency of the lysosomal enzyme , acid maltase / acid α-1,4 glucosidase ( GAA(passive) caused bya glycogen storage disease
Abstract : Muscle - specific deficiency of phosphorylase kinase ( Phkcausesglycogen storage disease
a deficiency of the enzyme a-1,4-glucosidase(passive) caused bya lysosomal glycogen storage disease
a deficiency in acid α - glucosidase ( GAA ) , a hydrolase necessary for the degradation of lysosomal glycogen(passive) caused bya glycogen storage disease
516–526 ( 2003 ) | Download Citation Muscle - specific deficiency of phosphorylase kinase ( Phkcausesglycogen storage disease
a rare deficiency in glucose-6-phosphatase or in amylo-1,6-glucosidase(passive) is caused byGlycogen storage disease
mutations in the PYGM gene encoding myophosphorylase(passive) caused bya glycogen storage disease
a genetically induced deficiency of the enzyme glucose-6-phosphatase(passive) caused byglycogen storage disease
a genetic deficiency of one or another of the enzymes of glycogen metabolism(passive) are caused byGlycogen storage diseases
an inherited deficiency in myophosphorylase , an enzyme that initiates the breakdown of muscle glycogen for glycolysis(passive) caused bya glycogen storage disease
a deficiency of lysosomal a - glucosidase(passive) caused byA glycogen storage disease
deficiency in a ( 1 4(passive) caused bySevere glycogen storage disease
Carlie Rider Etiology of GSD(passive) Created byGlycogen Storage Disease
At least 85 mutations in the G6PC gene have been foundto causeglycogen storage disease type
Deficiencies in PFK activitycan resultin the glycogen storage disease
apart from enzyme deficienciesmay leadto glycogen storage disease
Mao - Sen Sun , C Q Pan , +6 authors Janice Y Chou Deficiency of glucose-6-phosphatase ( G6Pase ) , a key enzyme in glucose homeostasiscausesglycogen storage disease type
an enzyme deficiency that prevents glycogenolysis and release of glucose into the circulation(passive) are caused byGlycogen storage diseases
deficiency of amylo-1,4 - 1,6 transglucosidase(passive) caused byglycogen storage disease
uric acid ( a waste product ) to accumulate in the joints , which can cause gout ( see Goutto causeuric acid ( a waste product ) to accumulate in the joints , which can cause gout ( see Gout
low blood sugar levelscauselow blood sugar levels
Melanie to have low blood sugarcausesMelanie to have low blood sugar
uric acid ( a waste product ) to accumulate in the joints , which can cause gout , and in the kidneys , which can cause kidney stonesto causeuric acid ( a waste product ) to accumulate in the joints , which can cause gout , and in the kidneys , which can cause kidney stones
in enlarged livers and low blood sugar Jan 27 , 2015can resultin enlarged livers and low blood sugar Jan 27 , 2015
persons with hypoglycemia(passive) caused bypersons with hypoglycemia
hepatosplenomegaly and failure to thrive Aguecheek diseasecausinghepatosplenomegaly and failure to thrive Aguecheek disease
accumulation of glycogen on cardiac tissuescausesaccumulation of glycogen on cardiac tissues
the body from using sugars properlypreventthe body from using sugars properly
hepatomegaly , cardiomegaly , muscle hypotonia , and deathcauseshepatomegaly , cardiomegaly , muscle hypotonia , and death
from known defects in glycogenolysis , glycolysis , and glycogen synthesis that have been described in humans and domestic animalsresultingfrom known defects in glycogenolysis , glycolysis , and glycogen synthesis that have been described in humans and domestic animals
in hypoglycemia and glycogen buildup in the liver that interferes with fat metabolismresultingin hypoglycemia and glycogen buildup in the liver that interferes with fat metabolism
glucose to build up in the body , leading to serious health issuescausesglucose to build up in the body , leading to serious health issues
the body to stop process glycogen , which is a sugar converted to glucose and is used by the body as energycausesthe body to stop process glycogen , which is a sugar converted to glucose and is used by the body as energy
to glycogenesis ( many typesleadsto glycogenesis ( many types
from enzyme deficiencies involving the glycolytic pathwayresultfrom enzyme deficiencies involving the glycolytic pathway
from the inability to properly metabolize glycogenresultfrom the inability to properly metabolize glycogen
filter results by(passive) are causedfilter results by
from genetically inherited deficiencies in enzymes required for glycogen synthesis or catabolismresultfrom genetically inherited deficiencies in enzymes required for glycogen synthesis or catabolism
glycogen to be stored every where - including the heart Compare and contrast dystrophic calcification with metastatic calcificationcausesglycogen to be stored every where - including the heart Compare and contrast dystrophic calcification with metastatic calcification
from the faulty processing of glycogen , which is a form of carbohydrateresultingfrom the faulty processing of glycogen , which is a form of carbohydrate
to glycogen deficiencyleadingto glycogen deficiency
glycogen ... the stored form of glucosepreventglycogen ... the stored form of glucose
GSD ) type IVcausesGSD ) type IV
from at least 10 different genetic defects in proteins required by glycogen metabolismresultfrom at least 10 different genetic defects in proteins required by glycogen metabolism
PGM1 ... Congenital disorder of deglycosylation 615273 ; Glycogen storage disease type XIV ( Glycogen storage disorders ) ; Congenital disorder of glycosylation , type It , 614921 ; Glycogen Storage Disorders- Muscle ; Glycogen Storage Disease Type XIV ; Glycogen storage disease XIV , 612934(passive) were setPGM1 ... Congenital disorder of deglycosylation 615273 ; Glycogen storage disease type XIV ( Glycogen storage disorders ) ; Congenital disorder of glycosylation , type It , 614921 ; Glycogen Storage Disorders- Muscle ; Glycogen Storage Disease Type XIV ; Glycogen storage disease XIV , 612934
from deficiencies in the enzymes that build glycogen , as well as those that interfere with the degradation of glycogen and subsequent mobilization of glucoseresultfrom deficiencies in the enzymes that build glycogen , as well as those that interfere with the degradation of glycogen and subsequent mobilization of glucose
from the congenital absence of various enzymesresultfrom the congenital absence of various enzymes
her to be hypoglycemiccausesher to be hypoglycemic
This was suspected(passive) to be caused byThis was suspected
to low glucose levels creating a metabolic condition known as reactive hypo - glycemiamay contributeto low glucose levels creating a metabolic condition known as reactive hypo - glycemia
to heart failuremay eventually leadto heart failure
Type 4causesType 4
GYS2 ... Glycogen storage disease , type 0 , 240600 ; fasting intolerance without enlarged liver(passive) were setGYS2 ... Glycogen storage disease , type 0 , 240600 ; fasting intolerance without enlarged liver
typicallycausetypically
PHKA2(passive) were setPHKA2
FSGS [ 40 , 41to causeFSGS [ 40 , 41
muscle weakness and exercise intolerance in young dogs and catscan causemuscle weakness and exercise intolerance in young dogs and cats
from a genetic enzyme deficiencyresultingfrom a genetic enzyme deficiency
to weakness , stiffness , exercise intolerance and difficulty swallowingcan leadto weakness , stiffness , exercise intolerance and difficulty swallowing