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categoría genética o congénita, neurología frecuencia poco común (U.S.) Usually seen in adults.

riesgo por la edad

riesgo por la duración de los síntomas

otros tipos médico family practitioner internist neurologist neurosurgeon código postal Buscar local Los resultados generados por computadora son sugerencias para ayudarle a encontrar un médico. MEDgle no recomienda ningún tipo de médico o pretenden ser completos o precisos en los proveedores y sugirió especialidades.

ataxias hereditarias, adulto tipo - trastornos hereditarios de coordinación Definición de ataxias hereditarias, adulto tipo http://www.mayoclinic.com/health/ataxia/DS00910/DSECTION=3 algunos síntomas comunes movimientos limitados pierna mala coordinación repentina incapacidad para moverse temblor algunos diagnósticos relacionados 1 - 7 of 31 diagnósticos Parkinsonismo la esclerosis múltiple polineuropatía neuropatía hereditaria motora y sensorial 1-3 adultos la enfermedad de Huntington lesiones cerebelosas Lewy enfermedad de los cuerpos   más do i have 'ataxias hereditarias, adulto tipo'? Además las siguientes pruebas de diagnóstico puede ser necesario para ayudar a verificar el diagnóstico: prueba de diagnóstico de los resultados de la búsqueda 'ataxias hereditarias, adulto tipo' 1 - 5 of 12 pruebas de diagnóstico Los estudios genéticos moleculares ataxias hereditarias, adulto tipo y Los estudios genéticos moleculares Niveles séricos de vitamina B-12 ataxias hereditarias, adulto tipo y Niveles séricos de vitamina B-12 Heavy metal de pantalla ataxias hereditarias, adulto tipo y Heavy metal de pantalla RM cerebral ataxias hereditarias, adulto tipo y RM cerebral CT del cerebro ataxias hereditarias, adulto tipo y CT del cerebro Ecocardiograma ataxias hereditarias, adulto tipo y Ecocardiograma ECG Electrocardiogram ataxias hereditarias, adulto tipo y ECG Electromiograma EMG ataxias hereditarias, adulto tipo y Electromiograma EMG Nervio NCS estudios de conducción ataxias hereditarias, adulto tipo y Nervio NCS estudios de conducción Conteo sanguíneo completo ataxias hereditarias, adulto tipo y Conteo sanguíneo completo Un análisis de orina Examination of urine to detect disease ataxias hereditarias, adulto tipo y Un análisis de orina Tomografía computarizada ataxias hereditarias, adulto tipo y Tomografía computarizada para obtener más ingreso por favor, es de acceso libre (haga clic aquí para acceder) procedimientos terapéuticos para 'ataxias hereditarias, adulto tipo'? La gestión o tratamiento de enfermedades debe ser siempre determinada por un proveedor de servicios de salud los pacientes. Abajo hay una lista de asociados procedimientos terapéuticos o medicamentos para hereditary ataxias, adult type: resultados terapéuticos procedimiento de buscar 'ataxias hereditarias, adulto tipo' 1 - 3 of 3 procedimientos terapéuticos clasificación son generadas por ordenador. por favor consulte a su proveedor de atención médica. Ortopedia Cuidado Quirúrgico ataxias hereditarias, adulto tipo y Ortopedia Cuidado Quirúrgico Arriostre ataxias hereditarias, adulto tipo y Arriostre bastones y andadores ataxias hereditarias, adulto tipo y bastones y andadores medicamentos para los resultados de la búsqueda 'ataxias hereditarias, adulto tipo' clasificación son generadas por ordenador. por favor consulte a su proveedor de atención médica. resultados de la búsqueda web para ataxias hereditarias, adulto tipo Web (Todos)  |  Tratamiento  |  Droga  |  Pruebas  |  Investigación  |  Dieta Resultados 1 - 50 - las ataxias hereditarias, el tipo de adultos Citrullinemia - Genetics Home Reference [Traducir esta página] The features of adult-onset type II citrullinemia may also develop in people who ... as lethargy, seizures, and ataxia) that are often seen in type I citrullinemia. ... http://ghr.nlm.nih.gov/condition=citrullinemia   ghr.nlm.nih.gov - summary Hereditary Ataxia Overview -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Protein kinase C gamma type. Non-repeat mutations ... Adult-onset ataxia, especially in men, may be part of the fragile X-associated ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ataxias   www.ncbi.nlm.nih.gov - summary WebMD Health A-Z - Find reliable health and medical information on ... [Traducir esta página] Helping older adults who are grieving. Helping teens who are grieving ... Hereditary Alkaptonuria. Hereditary Areflexic Dystasia. Hereditary Ataxia Friedrich's Type ... http://www.webmd.com/a-to-z-guides/health-topics/ha-he.htm   www.webmd.com - summary CDC's Hemochromatosis for Health Care Professionals [Traducir esta página] Hemochromatosis Type 1 (Adult) HFE gene mutations. Autosomal recessive. Hemochromatosis Type 2A ... Hereditary X-linked sideroblastic anemia. d-ALA synthase ... http://www.cdc.gov/ncbddd/hemochromatosis/training/pathophys...   www.cdc.gov - summary Blood/lymphatic system - Genetics Home Reference [Traducir esta página] basal ganglia disease, adult-onset see neuroferritinopathy ... Hereditary lymphedema type I see Milroy disease ... oculocutaneous see ataxia-telangiectasia ... http://ghr.nlm.nih.gov/ghr/conditionsByCategory/show/bloodlymphaticsystem   ghr.nlm.nih.gov - summary Spinocerebellar Ataxia Type 1 -- GeneReviews -- NCBI Bookshelf [Traducir esta página] In adult-onset SCA1, the duration of illness from onset to death ranges from ten ... A family with hereditary ataxia: HLA typing. Neurology. 1980; 30: 12?20. [PubMed] ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sca1   www.ncbi.nlm.nih.gov - summary Eyes and vision - Genetics Home Reference [Traducir esta página] congenital hereditary hematuria see Alport syndrome ... spinocerebellar ataxia, recessive, non-Friedreich type 1 see ataxia with oculomotor apraxia ... http://ghr.nlm.nih.gov/ghr/conditionsByCategory/show/eyesandvision   ghr.nlm.nih.gov - summary Ataxia: Causes - MayoClinic.com [Traducir esta página] Hereditary ataxias. Some types of ataxia and some conditions that cause ataxia are hereditary. ... Adult ataxia information for patients and caregivers. ... http://www.mayoclinic.com/health/ataxia/DS00910/DSECTION=causes   www.mayoclinic.com - summary -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Ataxia with Oculomotor Apraxia Type 2 AOA2 Maria-Céu Moreira and Michel Koenig ... Marie-Tooth Neuropathy Type 1 CMT1, HMSN1, Hereditary Motor and Sensory ... http://www.ncbi.nlm.nih.gov/books/bv.fcgi?call=bv.View..ShowTOC&rid=gene.TOC   www.ncbi.nlm.nih.gov - summary Heart and circulation - Genetics Home Reference [Traducir esta página] Hereditary spinal ataxia see Friedreich ataxia. Hereditary Spinal Sclerosis see Friedreich ataxia ... Hunter Syndrome see mucopolysaccharidosis type II ... http://www.ghr.nlm.nih.gov/ghr/conditionsByCategory/show/heartandcirculation   www.ghr.nlm.nih.gov - summary Lymphocytopenia: White Blood Cell Disorders: Merck Manual Home Edition [Traducir esta página] The number of specific types of lymphocytes (T lymphocytes, B lymphocytes, and ... People with a hereditary immunodeficiency may benefit from bone marrow (stem ... http://www.merck.com/mmhe/print/sec14/ch174/ch174d.html   www.merck.com - summary Skin, hair, and nails - Genetics Home Reference [Traducir esta página] Adult premature aging syndrome see Werner syndrome. Adult Progeria see Werner ... hereditary leiomyomatosis and renal cell cancer ... neurofibromatosis type 1 ... http://ghr.nlm.nih.gov/conditionCategory=skinhairandnails   ghr.nlm.nih.gov - summary Spinocerebellar Ataxia Type 2 -- GeneReviews -- NCBI Bookshelf [Traducir esta página] ... diagnosis of adult-onset sporadic progressive ataxia, multiple ... euro-ataxia (European Federation of Hereditary Ataxias) Boherboy, Dunlavin. Co Wicklow ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sca2   www.ncbi.nlm.nih.gov - summary Bones, muscles, and connective tissues - Genetics Home Reference [Traducir esta página] Autosomal Dominant Hereditary Spastic Paraplegia see spastic paraplegia type 4 ... Hereditary spinal ataxia see Friedreich ataxia ... http://ghr.nlm.nih.gov/ghr/conditionsByCategory/show/bonesmu...   ghr.nlm.nih.gov - summary Spinocerebellar Ataxia Type 3 -- GeneReviews -- NCBI Bookshelf [Traducir esta página] ... later adult onset often have a disorder that combines ataxia, generalized ... Hereditary spastic paraplegia and hereditary ataxia, Part 2: A family ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sca3   www.ncbi.nlm.nih.gov - summary Health Encyclopedia from A to Z on Yahoo! Health [Traducir esta página] Health encyclopedia of diseases and conditions covering signs, symptoms, causes, incidence, risk, prevention, tests, diagnosis, treatment, complications and side effects. http://health.yahoo.com/ency/   health.yahoo.com - summary Brain and nervous system - Genetics Home Reference [Traducir esta página] ataxia-telangiectasia. Ataxia with Lactic Acidosis, Type II see pyruvate ... Autosomal Dominant Hereditary Spastic Paraplegia see spastic paraplegia type 4 ... http://ghr.nlm.nih.gov/ghr/conditionsByCategory/show/brainandnervoussystem   ghr.nlm.nih.gov - summary Leber Hereditary Optic Neuropathy [Traducir esta página] ... (LHON) typically presents in young adults as bilateral, ... mutation type on clinical expression of Leber hereditary optic neuropathy. Am J Ophthalmol. ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary Cytarabine [Traducir esta página] Slurred speech and difficulty walking (ataxia) ... Is Colon Cancer Hereditary? ... Type 2 Diabetes? ... http://www.webmd.com/cancer/cytarabine   www.webmd.com - summary Leber's hereditary optic neuropathy - Wikipedia, the free encyclopedia [Traducir esta página] ... loss of central vision; this affects predominantly young adult males. ... The particular mutation type may predict likelihood of penetrance, severity of ... http://en.wikipedia.org/wiki/Leber's_hereditary_optic_neuropathy   en.wikipedia.org - summary OMIM Update List for March, 2004 [Traducir esta página] 158590 NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE II ... 108650 ATAXIA, SPASTIC, WITH CONGENITAL MIOSIS ... 601068 EPILEPSY, MYOCLONIC, BENIGN ADULT FAMILIAL, TYPE 1 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.2004   www.ncbi.nlm.nih.gov - summary OMIM Update List for July, 1996 [Traducir esta página] Clinical Synopsis for 125310 DEMENTIA, HEREDITARY MULTI-INFARCT TYPE ... Clinical Synopsis for 146300 HYPOPHOSPHATASIA, ADULT TYPE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?7.1996   www.ncbi.nlm.nih.gov - summary Deafness and Hereditary Hearing Loss Overview -- GeneReviews -- NCBI ... [Traducir esta página] ... average threshold for a normal hearing adult; 120 dB HL is so loud as ... genetics of common syndromic and nonsyndromic types of hereditary hearing loss. ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=deafness-overview   www.ncbi.nlm.nih.gov - summary Spastic Paraplegia Type 11 [Traducir esta página] [Includes: SPG11-Related Hereditary Spastic Paraplegia with Thin Corpus Callosum ... National Ataxia Foundation. 2600 Fernbrook Lane Suite 119. Minneapolis MN 55447 ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary Hereditary generalized amyloidosis with polyneuropathy ... [Traducir esta página] ... common form of hereditary generalized amyloidosis in Japan is type I FAP, but ... Adult. Aged. Amyloidosis/diagnosis. Amyloidosis/genetics* Amyloidosis/pathology ... http://www.ncbi.nlm.nih.gov/pubmed/3032328   www.ncbi.nlm.nih.gov - summary Parkinson's Disease: Challenges, Progress, and Promise: National ... [Traducir esta página] ... revealed a potential link between hereditary and sporadic forms of the disease ... the midbrain, cerebellum, brainstem, and spinal cord and develop an adult-onset ... http://www.ninds.nih.gov/disorders/parkinsons_disease/parkinsons_research.htm   www.ninds.nih.gov - summary MedlinePlus Medical Encyclopedia: Topics beginning with A-Ag [Traducir esta página] Abnormality of the urea cycle - hereditary see Hereditary urea cycle abnormality ... Adult-onset diabetes see Type 2 diabetes. Adult Still's disease ... http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_A-Ag.htm   www.nlm.nih.gov - summary OMIM Update List for August, 1996 [Traducir esta página] 162400 NEUROPATHY, HEREDITARY SENSORY, TYPE 1; HSN1 ... 158590 MUSCULAR ATROPHY, ADULT SPINAL. 188826 TISSUE INHIBITOR OF METALLOPROTEINASE-3; TIMP3 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?8.1996   www.ncbi.nlm.nih.gov - summary Diabetes mellitus - Wikipedia, the free encyclopedia [Traducir esta página] ... term "type 2 diabetes" has replaced several former terms, including adult-onset ... Various hereditary conditions may feature diabetes, for example myotonic ... http://en.wikipedia.org/wiki/Diabetes_mellitus   en.wikipedia.org - summary OMIM Update List for August, 2005 [Traducir esta página] 609065 CEREBRAL HEMORRHAGE WITH AMYLOIDOSIS, HEREDITARY, DUTCH TYPE ... 223100 HYPOLACTASIA, ADULT TYPE. 234200 PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATION; PKAN ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?8.2005   www.ncbi.nlm.nih.gov - summary Charcot-Marie-Tooth Neuropathy Type 1 -- GeneReviews -- NCBI Bookshelf [Traducir esta página] The typical adult individual has bilateral foot drop, symmetrical atrophy of ... Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=cmt1   www.ncbi.nlm.nih.gov - summary Episodic Ataxia Type 2 -- GeneReviews -- NCBI Bookshelf [Traducir esta página] ... by adult-onset, slowly progressive cerebellar ataxia, dysarthria, and ... Hereditary myokymia and paroxysmal ataxia linked to chromosome 12 is responsive ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ea2   www.ncbi.nlm.nih.gov - summary Hereditary Hemorrhagic Telangiectasia -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Hereditary hemorrhagic telangiectasia type 2 (HHT2) ... Ataxia-telangiectasia, which is characterized by progressive cerebellar ataxia ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=hht   www.ncbi.nlm.nih.gov - summary Haemochromatosis - Wikipedia, the free encyclopedia [Traducir esta página] Those with hereditary anemias such as beta-thalassemia major, sickle cell anemia, ... Haemochromatosis type 4 autosomal dominant haemochromatosis (all others are ... http://en.wikipedia.org/wiki/Haemochromatosis   en.wikipedia.org - summary Hemochromatosis for Health Care Professionals [Traducir esta página] The majority of hereditary hemochromatosis (also known as Type 1 ... This online course focuses on adult onset HFE hereditary hemochromatosis. ... http://www.cdc.gov/ncbddd/hemochromatosis/training/pdf/hemoc...   www.cdc.gov - summary Tyrosinemia Type 1 -- GeneReviews -- NCBI Bookshelf [Traducir esta página] ... reproductive options) to young adults who are affected, are carriers, or are at ... Different clinical forms of hereditary tyrosinemia (type I) in patients with ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tyrosinemia   www.ncbi.nlm.nih.gov - summary List of diseases (H) - Wikipedia, the free encyclopedia [Traducir esta página] Harding ataxia. Harlequin type ichthyosis. Harpaxophobia. Harrod Doman ... Heart hand syndrome Spanish type. Heart hypertrophy, hereditary. Heart situs anomaly ... http://en.wikipedia.org/wiki/List_of_diseases_(H)   en.wikipedia.org - summary Restless legs syndrome and related disorders [Traducir esta página] ... common type of arthritis affecting mostly older adults. Varicose veins. ... Hereditary ataxia, a group of genetic diseases that affects the central nervous ... http://adam.about.com/reports/Restless-legs-syndrome-and-related-disorders.htm   adam.about.com - summary Hereditary Spastic Paraplegia Overview -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Familial adult onset of Krabbe's disease resembling hereditary spastic ... Classification of the hereditary ataxias and paraplegias. Lancet. 1983; 1: 1151?5. ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=hsp   www.ncbi.nlm.nih.gov - summary BRCA1 and BRCA2 Hereditary Breast/Ovarian Cancer [Traducir esta página] prenatal diagnosis of adult-onset diseases are uncommon and require ... isolated cell type carcinoma. The average age of onset of hereditary diffuse gastric ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary Spinocerebellar Ataxia Type 17 [Traducir esta página] in adults and ataxia, myoclonus, epilepsy, and progressive intellectual ... euro-ataxia (European Federation of Hereditary Ataxias) Boherboy Dunlavin. Co Wicklow ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary 16609806 2006 10 05 2007 03 13 0340-5354 253 9 2006 Sep J. Neurol ... [Traducir esta página] Spinocerebellar ataxia type 2 olfactory impairment shows a pattern similar to ... has been found that some hereditary ataxias are also associated with significant ... http://www.ncbi.nlm.nih.gov/pubmed/16609806?dopt=Abstract   www.ncbi.nlm.nih.gov - summary Cerebellar ataxia in patients with Leber's hereditary optic neuropathy. [Traducir esta página] Publication Types: Case Reports. Mesh Terms: Adult. Cerebellar Ataxia/complications* DNA, Mitochondrial/genetics. Female. Humans. Male ... http://www.ncbi.nlm.nih.gov/pubmed/7707093   www.ncbi.nlm.nih.gov - summary List of diseases (N) - Wikipedia, the free encyclopedia [Traducir esta página] Nephrolithiasis type 2. Nephronophthisis familial adult spastic quadriparesis ... hereditary motor and sensory, LOM type. Neuropathy, hereditary sensory, type ... http://en.wikipedia.org/wiki/List_of_diseases_(N)   en.wikipedia.org - summary OMIM Update List for April, 2008 [Traducir esta página] 611955 PROSTATE CANCER, HEREDITARY, 11; HPC11 ... 601068 EPILEPSY, MYOCLONIC, BENIGN ADULT FAMILIAL, TYPE 1 ... 160120 EPISODIC ATAXIA, TYPE 1; EA1 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?4.2008   www.ncbi.nlm.nih.gov - summary Spinal muscular atrophy - Wikipedia, the free encyclopedia [Traducir esta página] Type 4: "Adult" 271150 [edit] SMA Caused by mutation of other genes ... ataxia (Friedreich's ataxia, Ataxia telangiectasia, Hereditary spastic paraplegia) ... http://en.wikipedia.org/wiki/Spinal_muscular_atrophy   en.wikipedia.org - summary OMIM Update List for May, 1996 [Traducir esta página] 182900 SPHEROCYTOSIS, HEREDITARY; HS. 183600 SPLIT-HAND/FOOT DEFORMITY, TYPE I; SHFD1 ... 601238 CEREBELLAR ATAXIA, CAYMAN TYPE. 601239 DYSTOBREVIN ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?5.1996   www.ncbi.nlm.nih.gov - summary Dementia: Hope Through Research - NINDS [Traducir esta página] Another type of vascular dementia is linked to a rare hereditary disorder called ... Symptoms of GSS typically include ataxia and progressive dementia that begins ... http://www.ninds.nih.gov/disorders/dementias/detail_dementia.htm   www.ninds.nih.gov - summary OMIM Update List for May, 1999 [Traducir esta página] 603471 CITRULLINEMIA, ADULT-ONSET TYPE II; CTLN2 ... 103580 ALBRIGHT HEREDITARY OSTEODYSTROPHY; AHO. 104530 AMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?5.1999   www.ncbi.nlm.nih.gov - summary MIM Morbid map [Traducir esta página] Polycystic kidney disease, adult, type II (3) PKD2, PKD4. 173910. 4q21-q23 ... Polyposis syndrome, hereditary mixed, 2, 610069 (3) BMPR1A, ACVRLK3, ALK3 ... http://www.ncbi.nlm.nih.gov/Omim/getmorbid.cgi?start=3307   www.ncbi.nlm.nih.gov - summary mostrar más 1  2