en Anglais
af Afrikaanssq Albanaisam Amharicar Arabehy Arménienaz Azerbaïdjanaiseu Basquebe Biélorussebn Bengalibs Bosnienbg Bulgareca Catalanceb Cebuanony Chichewazh-CN Chinois (simplifié)zh-TW Chinois (traditionnel)co Corsehr Croatecs Tchèqueda Danoisnl Néerlandaisen Anglaiseo Esperantoet Estonientl Philippinfi En finnoisfr Françaisfy Frisongl Galicienka Géorgiende Allemandel Grecgu Gujaratiht Créole haïtienha Hausahaw Hawaïenneiw En hébreuhi Hindihmn Hmonghu Hongroisis Islandaisig Igboid Indonésienga Irlandaisit Italienja Japonaisjw Javanaiskn Kannadakk Kazakhkm Khmerko Coréenku Kurde (Kurmanji)ky Kirghizelo Laola Latinlv Lettonlt En lituanienlb En luxembourgeoismk Macédonienmg Malgachems Malaisml Malayalammt Maltaismi Maorimr Marathimn Mongolmy Myanmar (Birmanie)ne Népalaisno Norvégienps Pachtounefa Persanpl Polonaispt Portugaispa Punjabiro En roumainru Russesm Samoangd Gaélique écossaissr Serbest Sesothosn Shonasd Sindhisi Sinhalask Slovaquesl Slovèneso Somalienes Espagnolsu Soudanaissw Swahilisv Suédoistg Tadjikta Tamilte Teluguth Thaitr Turcuk Ukrainienur Urduuz Ouzbékistanvi Vietnamiency Galloisxh Xhosayi Yiddishyo Yorubazu Zulu

DISEASES THAT
MIMIC MSA

GENETIC MSA-MIMICKING DISEASES,  SUBTYPES & OTHER DISORDERS

Ataxias

      • Spinocerebellar Ataxias (Genetic Forms)
      • Dentatorubral-pallidoluysian atrophy (DRPLA)
      • fragile X-associated tremor/ataxia syndrome (FXTAS)
      • Friedreich Ataxia (FRDA)
      • Ataxia-oculomotor apraxia syndrome (AOA)
      • Ataxia with vitamin E deficiency (AVED)
      • Marinesco Sjogren syndrome (SIL1 mutation)
      • Alexanders syndrome

Parkinsonism

      • Perry syndrome
      • Huntington’s disease
      • Familial Parkinson’s Disease with the SNCA gene (FPD)
      • Familial Parkinson’s Disease with the LRRK2 gene (FPD)
      • Familial Parkinson’s Disease with the GBA gene (FPD)
      • X-linked adrenoleukodystrophy (ABCD1 mutation)

Spastic gait

      • Hereditary Spastic Paraplegia (HSP)
      • Hereditary Spastic Paraplegia Paraplegin (SPG7)
      • Hereditary Spastic Paraplegia Mental Impairment and Thin Corpus Callosum (SPG11)
      • Primary Lateral Sclerosis (PLS)

Autonomic failure

      • LMNB1 associated Leukodystrophy

Complex phenotypes

      • Mitochondriopathy
      • Cerebrotendinous xanthomatosis
      • Prion disease
      • C9ORF72 mutation

OTHER DISORDERS

Non-Acquired

      • Dementia with Lewy Bodies
      • Progressive Supranuclear Palsy
      • Parkinson’s Disease
      • Pure autonomic failure (however there are some ideas that this entity is a spectrum)
      • Corticobasal degeneration
      • Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS)
      • Vascular parkinsonism
      • Normal pressure hydrocephalus
      • Prion disorder (genetic or sporadic)

Acquired

      • Whipple’s disease
      • Extrapontine myelinolysis
      • Paraneoplastic cerebellar degeneration
      • Alcoholic cerebellar degeneration
      • Drug-induced cerebellar degeneration
      • Gluten Ataxia

Search Directory of Genetic and Rare Diseases Information Center (GARD) provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish.

Alphabetical List of Rare Diseases National Organization of Rare Diseases (NORD)

 

Prepared By:

Dr. Oybek E. Turgunkhujaev (Defeat MSA Consulting Neurologist – Movement Disorders)

Interdisciplinary Rehabilitation Center (IRC)

117628, Moscow, Starobittsevskaya St 23, building 2

 

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