Loading ...
Conditionscould causeAcute cerebellar ataxia
mutations in metabotropic glutamate receptor 1(passive) is caused bycongenital cerebellar ataxia
genetics , viral infections , autoimmune disorders , or injury(passive) may be caused byAcute cerebellar ataxia
the use the viruscausesencephalopathy , cerebellar ataxia
A mutation in the * TDP1 * genecausesspinocerebellar ataxia
by a mutation in the ATXN3 gene(passive) caused byspinocerebellar ataxia
cerebellar development ... , and missense mutations incausingcerebellar ataxia
by recessive mutations in mitochondrial proteins(passive) is causedspinocerebellar ataxia
by recessive mutations in mitochondrial proteins(passive) is caused byspinocerebellar ataxia
trinucleotide repeat gene ... ( SCA7causingspinocerebellar ataxia
the mutant genecausesspinocerebellar ataxia
Expansion of a CAG repeat in the coding regioncausesspinocerebellar ataxia
the genecausesspinocerebellar ataxia
genecausesspinocerebellar ataxia
the genecausingspinocerebellar ataxia
Most mutationscausespinocerebellar ataxia
The trinucleotide repeat expansion in this exoncausesspinocerebellar ataxia
cerebellar disease(passive) is ataxia caused byThe cerebellar ataxia
by recessive mutations(passive) is causedspinocerebellar ataxia
by recessive mutations(passive) is caused byspinocerebellar ataxia
Spectrin mutationscausespinocerebellar ataxia
mutations in AFG3L2causespinocerebellar ataxia
damage to the cerebellumdoes ... causecerebellar ataxia
the different mutationscausingspinocerebellar ataxia
Identification of the genecausingspinocerebellar ataxia
Vitamin E deficiency has been shownto causespinocerebellar ataxia
expansioncausingspinocerebellar ataxia
the mutant genecausescerebellar ataxia
by cerebellar lesions(passive) caused bycerebellar ataxia
dysfunction of the cerebellum(passive) is ataxia caused byCerebellar ataxia
loss - of - function mutations in TDP1may causespinocerebellar ataxia
White matter damage in the cerebellumcausescerebellar ataxia
the degeneration of the cerebellum(passive) is caused byCerebellar Ataxia
by the expansion of the intronic GGCCTG hexanucleotide repeat in NOP56(passive) is caused bySpinocerebellar ataxia
knownto causespinocerebellar ataxia
the impairment of Purkinje cellscausescerebellar ataxia
compression of the brain ... cerebellar atrophycausescerebellar ataxia
the abnormal repeatscausespinocerebellar ataxia
Introduction Cerebellar ataxiacausesCerebellar ataxia
one copy of the normal gene and one copy of the mutant genecausescerebellar ataxia
due to strokecauseddue to stroke
an inability to coordinate muscle movementscausesan inability to coordinate muscle movements
in disorders in fine movement , posture , and motor learning in humanscan resultin disorders in fine movement , posture , and motor learning in humans
alsocan ... resultalso
alsocan ... resultalso
to the patientleadingto the patient
to impaired motor coordinationleadsto impaired motor coordination
uncoordinated movement and muscle tremorscausesuncoordinated movement and muscle tremors
in impaired coordinationresultsin impaired coordination
to a number of symptoms , such as : a wide and unsteady gait when walkingcan leadto a number of symptoms , such as : a wide and unsteady gait when walking
in unsteady gait , clumsiness , and dysarthriaresultingin unsteady gait , clumsiness , and dysarthria
unsteadiness and loss of co - ordinationcausesunsteadiness and loss of co - ordination
balance and coordination problems and difficulty talkingcausesbalance and coordination problems and difficulty talking
balance issuescausesbalance issues
in a characteristic type of irregular , uncoordinated movement nstability of gaitresultsin a characteristic type of irregular , uncoordinated movement nstability of gait
in a characteristic type of irregular , uncoordinated movement nstability of gaitresultsin a characteristic type of irregular , uncoordinated movement nstability of gait
in an unsteady gait and slurred speechresultsin an unsteady gait and slurred speech
with incoordination of movementcould resultwith incoordination of movement
to dysarthriacould also contributeto dysarthria
disturbance in balance leading to unsteadinesscausesdisturbance in balance leading to unsteadiness
to dizzinesscould contributeto dizziness
with incoordination of movement , particularly in the extremitiescould resultwith incoordination of movement , particularly in the extremities
Most often(passive) is causedMost often
by bilateral cortical atrophy of the cerebellumcausedby bilateral cortical atrophy of the cerebellum
to a loss of this particular reflexcan leadto a loss of this particular reflex
her head to shakecausesher head to shake
jerky movements , tremors and generally uncoordinated movementcausesjerky movements , tremors and generally uncoordinated movement
jerky movements , tremors and generally uncoordinated motioncausesjerky movements , tremors and generally uncoordinated motion
usuallycausesusually
jerky movements , tremors and generallycausesjerky movements , tremors and generally
jerky movements tremors andcausesjerky movements tremors and
jerky movements tremorscausesjerky movements tremors
coordination , and movement problemsonly causescoordination , and movement problems
motor issuescausesmotor issues
jerky movementscausesjerky movements
uncoordinated movementcan causeuncoordinated movement
him to have balance problemscauseshim to have balance problems
balance problems(passive) caused bybalance problems
Hydrocephalus and(passive) have been causedHydrocephalus and
an underdeveloped cerebellum in the brain , which controls all motor skillscausesan underdeveloped cerebellum in the brain , which controls all motor skills