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autosomal dominant cerebellar ataxia
Definition for autosomal dominant cerebellar ataxia
some common symptoms
some related diagnoses
do i have 'autosomal dominant cerebellar ataxia'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'autosomal dominant cerebellar ataxia'
1 - 1 of
1
diagnostic tests
Trinucleotide Repeat Analysis
autosomal dominant cerebellar ataxia and Trinucleotide Repeat Analysis
therapeutic procedures for 'autosomal dominant cerebellar ataxia'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for autosomal dominant cerebellar ataxia:
therapeutic procedure search results for 'autosomal dominant cerebellar ataxia'
rankings are computer generated. please consult your health care provider.
medications search results for 'autosomal dominant cerebellar ataxia'
rankings are computer generated. please consult your health care provider.
web search results for autosomal dominant cerebellar ataxia
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1 - 50
- autosomal dominant cerebellar ataxia
Spinocerebellar ataxia - Wikipedia, the free encyclopedia
There are numerous types of autosomal dominant cerebellar ataxias. There are five typical autosomal recessive disorders in which ataxia is a prominent feature ...
http://en.wikipedia.org/wiki/Spinocerebellar_ataxia
en.wikipedia.org
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Ataxia, Hereditary, Autosomal Dominant - Yahoo! Health
ImportantIt is possible that the main title of the report Ataxia, Hereditary, Autosomal Dominantis not the name you expected.
http://health.yahoo.com/nervous-overview/ataxia-hereditary-a...
health.yahoo.com
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Ataxia, Hereditary, Autosomal Dominant
Important It is possible that the main title of the report Ataxia, Hereditary, Autosomal Dominant is not the name you expected. Please check the synonyms listing to ...
http://www.webmd.com/brain/ataxia-hereditary-autosomal-dominant
www.webmd.com
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Spinocerebellar ataxia type-13 - Wikipedia, the free encyclopedia
Spinocerebellar ataxia type 13 (SCA13) is a rare autosomal dominant disorder, which, like ... An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of ...
http://en.wikipedia.org/wiki/Spinocerebellar_ataxia_type-13
en.wikipedia.org
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Spinocerebellar ataxia type-6 - Wikipedia, the free encyclopedia
Spinocerebellar ataxia type 6 (SCA6) is a rare, late-onset, autosomal dominant disorder, ... Autosomal dominant cerebellar ataxia (SCA6) associated with small ...
http://en.wikipedia.org/wiki/Spinocerebellar_ataxia_type-6
en.wikipedia.org
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Cerebellar Disorders: Movement and Cerebellar Disorders ...
Ataxia is the archetypal sign of cerebellar dysfunction, but many other motor ... Hereditary ataxias may be autosomal recessive or autosomal dominant. ...
http://www.merck.com/mmpe/print/sec16/ch221/ch221j.html
www.merck.com
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ATXN2 - NextBio
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration ...
http://www.nextbio.com/b/search/ov/ATXN2?type=feature&id=24501
www.nextbio.com
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Cerebellar Disorders: Movement and Cerebellar Disorders ...
Autosomal recessive ataxias include Friedreich's ataxia (the most prevalent), ataxia ... Spinocerebellar ataxias (SCAs) are the main autosomal dominant ataxias. ...
http://www.merck.com/mmpe/sec16/ch221/ch221j.html
www.merck.com
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Click here for an Excel file listing of available tissue samples
Retinitis pigmentosa, autosomal dominant inheritance, no vision for the past 20 yrs ... history of autosomal dominant cerebellar ataxia. Cone retinal ...
http://www.clevelandclinic.org/eye/docs/FFB_Jan2008.xls
www.clevelandclinic.org
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MACHADO-JOSEPH DISEASE - Pedbase.org
... degenerative disorder characterized by cerebellar dysfunction, pyramidal signs, and ophthalmoplegia. ... familial - autosomal dominant. chrom.#: 14q32.1. gene: ? Azores Islands ...
http://www.pedbase.org/m/machado-joseph-disease/
www.pedbase.org
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Olivopontocerebellar Atrophy - Yahoo! Health
ImportantIt is possible that the main title of the report Olivopontocerebellar Atrophyis not the name you expected.
http://health.yahoo.com/nervous-resources/olivopontocerebell...
health.yahoo.com
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Olivopontocerebellar Atrophy, Hereditary
Important It is possible that the main title of the report Olivopontocerebellar Atrophy, ... are discussed in detail in the NORD report on autosomal dominant hereditary ataxias. ...
http://www.webmd.com/brain/olivopontocerebellar-atrophy-hereditary
www.webmd.com
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Cacna1a - NextBio
Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia. ... Large CACNA1A deletion in a family with episodic ataxia type 2. ...
http://www.nextbio.com/b/search/ov/Cacna1a?type=feature
www.nextbio.com
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A
Acute cerebellar ataxia. Acute childhood leukemia. Acute cholecystitis. Acute confusional ... Autosomal dominant polycystic kidney disease. Axillary abscess ...
http://forthealthcare.adam.com/content.aspx?productId=105&pid=1&alpha=A
forthealthcare.adam.com
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a - Mary Greeley Medical Center
Ataxia - acute cerebellar. Ataxia - telangiectasia. Atelectasis. Atheroemboli - renal ... Autosomal dominant polycystic kidney disease. Avascular necrosis. Avian ...
http://mgmc.adam.com/content.aspx?productId=117&pid=1&alpha=a&sub=Disease
mgmc.adam.com
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A - Pfizer
Acute cerebellar ataxia. Acute childhood leukemia. Acute cholecystitis ... Autosomal dominant. Autosomal dominant polycystic kidney disease. Autosomal recessive ...
http://pfizer.adam.com/content.aspx?productId=101&alpha=A
pfizer.adam.com
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Test
Acute cerebellar ataxia. Acute childhood leukemia. Acute cholecystitis ... Autosomal dominant polycystic kidney disease © 1997- All rights reserved. Community ...
http://pricechopper.adam.com/content.aspx?productId=105&alpha=a&sub=Disease
pricechopper.adam.com
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Topics beginning with A: MedlinePlus Medical Encyclopedia
Acute cerebellar ataxia. Acute cholecystitis. Acute cytomegalovirus ... Autosomal dominant. Autosomal recessive. Avian influenza. Avoidant personality disorder ...
http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_A.htm
www.nlm.nih.gov
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Ataxia - Wikipedia
User-submitted article about ataxia, which is the unsteady and clumsy motion of the limbs or torso due to the failure of the coordination of muscle movements.
http://en.wikipedia.org/wiki/Ataxia
en.wikipedia.org
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Encyclopedia A-Az on Yahoo! Health
Health encyclopedia of diseases and conditions covering symptoms, definitions, alternative names, causes, incidence, risk factors, prevention, signs and tests, ...
http://health.yahoo.com/ency/
health.yahoo.com
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No title
Acute cerebellar ataxia. Acute childhood leukemia. Acute cholecystitis ... Autosomal dominant. Autosomal dominant polycystic kidney disease. Autosomal recessive ...
http://adam.about.com/encyclopedia/alphaidxa.htm
adam.about.com
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A - Alexian Brothers Health System
Acute cerebellar ataxia (Condition) Acute childhood leukemia ... (Condition) Autosomal dominant (Special Topic) Autosomal dominant polycystic kidney ...
http://alexianbrothershealth.adam.com/content.aspx?productId=26&alpha=A
alexianbrothershealth.adam.com
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a - Great Falls Clinic
Providing a number of clinical services to Great Falls, Montana and the surrounding areas. ... Ataxia - acute cerebellar. Ataxia - telangiectasia. Atelectasis. Atheroemboli - renal ...
http://gfclinic.adam.com/content.aspx?productId=117&pid=1&alpha=a&sub=Disease
gfclinic.adam.com
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SSM St. Joseph Hospital of Kirkwood Home Page
A member of SSM Health Care. Body, Mind, Spirit... We care for the whole person. ... Acute cerebellar ataxia. Acute childhood leukemia. Acute cholecystitis. Acute colonic ileus ...
http://ssmhealth.adam.com/content.aspx?pid=1&gid=200000&sub=...
ssmhealth.adam.com
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New Medical Subject Headings
A rare autosomal recessive disorder resulting from the absence of ... of the non-dominant hemisphere from language centers in the dominant hemisphere. ...
http://www.nlm.nih.gov/mesh/newh2000.html
www.nlm.nih.gov
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Index: CE: Merck Manual Professional
Cerebellar ataxia. Approach to the Neurologic Patient: Gait, stance, and coordination ... Autosomal Dominant Polycystic Kidney Disease (ADPKD): Pathophysiology ...
http://www.merck.com/mmpe/index/ind_ce.html
www.merck.com
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Episodic ataxia - Wikipedia, the free encyclopedia
Episodic ataxia (EA) is an autosomal dominant disorder characterized ... ataxia and acetazolamide-responsive hereditary paroxysmal cerebellar ataxia (AHPCA) ...
http://en.wikipedia.org/wiki/Episodic_ataxia
en.wikipedia.org
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Nova Scotia Department of Health
Acute cerebellar ataxia (Condition) Acute childhood leukemia (Condition) Acute ... (Condition) Autosomal dominant polycystic kidney disease (Condition) ...
http://novascotiadeptofhealth.adam.com/content.aspx?productId=26&alpha=A
novascotiadeptofhealth.adam.com
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MedTerms Medical Dictionary A-Z List - A
Ataxia, cerebellar. Ataxia-telangiectasia. ATCC (American Type Culture Collection) ... Autosomal dominant hereditary spastic paraplegia. Autosomal dominant ...
http://www.medicinenet.com/htmlalphaidx/dict_A.htm
www.medicinenet.com
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A
Acute cerebellar ataxia (Condition) Acute childhood leukemia (Condition) Acute ... Autosomal dominant polycystic kidney disease (Condition) [top] Ax ...
http://forthealthcare.adam.com/content.aspx?productId=26&pid=26&alpha=A
forthealthcare.adam.com
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NEUROBLASTOMA - Pedbase.org
a subset have an autosomal dominant pattern of inheritance ... 5.Progressive Cerebellar Ataxia. INVESTIGATIONS: 1. Imaging Studies. Chest X-Ray, Abdominal ...
http://www.pedbase.org/n/neuroblastoma/
www.pedbase.org
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Behr syndrome(Abortive cerebellar ataxia) - NextBio
Search Term: Behr syndrome (disease: Abortive cerebellar ataxia) ... Familial Behr syndrome-like phenotype with autosomal dominant inheritance. ...
http://www.nextbio.com/b/search/ov/Behr%20syndrome?type=DISEASE
www.nextbio.com
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Hypolipidemia: Lipid Disorders: Merck Manual Professional
... signs, and cerebellar signs of dysmetria, ataxia, and spasticity, ... Hypobetalipoproteinemia: Hypobetalipoproteinemia is an autosomal dominant or codominant condition caused by ...
http://www.merck.com/mmpe/sec12/ch159/ch159c.html
www.merck.com
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Sensory ataxia - Wikipedia, the free encyclopedia
Sensory ataxia also lacks the associated features of cerebellar ataxia such as pendular ... Autosomal dominant sensory ataxia: a neuroaxonal dystrophy" ...
http://en.wikipedia.org/wiki/Sensory_ataxia
en.wikipedia.org
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Hypolipidemia: Lipid Disorders: Merck Manual Professional
This is an autosomal recessive condition caused by mutations in the gene for microsomal ... column signs, and cerebellar signs of dysmetria, ataxia, and spasticity, which can ...
https://www.merck.com/mmpe/print/sec12/ch159/ch159c.html
/www.merck.com
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2008 MeSH Tree Structures. C10 - Nervous System Diseases
Paraneoplastic Cerebellar Degeneration [C10.228.140.252.620] ... Optic Atrophy, Autosomal Dominant [C10.292.700.225.500.100] Optic Atrophy, Hereditary, ...
http://www.nlm.nih.gov/mesh/trees2008/C10.html
www.nlm.nih.gov
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Test
Acetaminophen, sodium bicarbonate, and citric acid (Oral route) ... Acute cerebellar ataxia (Condition) Acute childhood leukemia (Condition) Acute ...
http://pricechopper.adam.com/content.aspx?productId=26&alpha=A
pricechopper.adam.com
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Nicola Migone - NextBio
BACKGROUND: Autosomal dominant cerebellar ataxias are a clinical and genetically ... onset, slowly progressive, autosomal dominant cerebellar ataxia. ...
http://www.nextbio.com/b/search/author/Nicola%20Migone
www.nextbio.com
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Ataxia: Causes - MayoClinic.com
Ataxia ? Comprehensive overview covers causes and treatments for this lack of muscle coordination.
http://www.mayoclinic.com/health/ataxia/DS00910/DSECTION=causes
www.mayoclinic.com
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Y Hashizume - NextBio
Spinocerebellar ataxia type 31 (SCA31) is an adult-onset autosomal-dominant neurodegenerative disorder showing progressive cerebellar ataxia mainly af...
http://www.nextbio.com/b/search/author/Y%20Hashizume
www.nextbio.com
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cerebellar ataxia - NextBio
Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to ...
http://www.nextbio.com/b/search/ov/cerebellar%20ataxia
www.nextbio.com
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Author - NextBio
Ataxia-ocular apraxia 2 (AOA2) was recently identified as a new autosomal recessive ataxia. We have now ... in European and North African autosomal dominant Parkinson's disease. ...
http://www.nextbio.com/b/search/author/C%20Tranchant
www.nextbio.com
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Loyola University Health System
myLoyola provides you a customized interaction with Loyola University Health System based on age group, gender, city and any medical interests you specify. ...
http://loyolauniversity.adam.com/content.aspx?productId=26&alpha=A
loyolauniversity.adam.com
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RANSMISSIBLE
autosomal dominant inheritance pattern, there is commonly a family ... patients include cerebellar ataxia, gait abnormalities, dementia, dysarthria, ocular ...
http://www.cdc.gov/ncidod/dvrd/vcjd/resources/BelayE_Annu_Rev_Microbio.pdf
www.cdc.gov
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H Yamanouchi - NextBio
An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 ... Autosomal dominant cerebellar ataxia (ADCA) is a group of heterogeneous neurodegenerative disorders. By ...
http://www.nextbio.com/b/search/author/H%20Yamanouchi
www.nextbio.com
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Joanna C Jen - NextBio
Autosomal dominant retinal vasculopathy with cerebral leukodystrophy is a ... Hereditary episodic ataxia (EA) syndromes are rare monogenic disorders that are ...
http://www.nextbio.com/b/search/author/Joanna%20C%20Jen
www.nextbio.com
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Author - NextBio
Spinocerebellar ataxia type 7 (SCA7) is an autosomal dominant cerebellar ataxia caused by a CAG repeat expansion in the ataxin-7 gene. In humans, SCA7...
http://www.nextbio.com/b/search/author/John%20P%20McAbney
www.nextbio.com
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Author - NextBio
Friedreich ataxia is an autosomal recessive degenerative disease that primarily ... dysfunction in autosomal dominant inherited spinocerebellar ataxias ...
http://www.nextbio.com/b/search/author/Massimo%20Pandolfo
www.nextbio.com
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VON HIPPEL-LINDAU DISEASE - Pedbase.org
all children presenting with cerebellar hemangioblastomas have VHL ... cerebellar hemangioblastomas appear as cystic lesions with a vascular mural ...
http://www.pedbase.org/v/von-hippel-lindau-disease/
www.pedbase.org
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ATXN2 - Wikipedia, the free encyclopedia
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of ... second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23 ...
http://en.wikipedia.org/wiki/ATXN2
en.wikipedia.org
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