Spinocerebellar Degenerations

A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked.

Also Known As:

Marinesco Sjogren Syndrome; Spinocerebellar Degeneration; Ataxia, Hereditary; Hereditary Ataxia; Syndrome, Marinesco-Sjogren; Early Onset Cerebellar Ataxia; Late Onset Cerebellar Ataxia; Spinocerebellar Diseases; Corticostriatal Spinal Degeneration; Hereditary Ataxias; Spinocerebellar Disease; Familial Spinocerebellar Degenerations; Garland-Moorhouse Syndrome; Hereditary Oligophrenic Cerebello-Lental Degeneration; Hereditary Spinocerebellar Degenerations; Inherited Spinocerebellar Degenerations; Marie's Cerebellar Ataxia; Marinesco-Garland Syndrome; Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism; Marinesco-Sjogren Syndrome-Myopathy; Marinesco-Sjogren-Garland Syndrome; Marinesco-Sjögren Syndrome; Spino Cerebellar Degenerations; Spino-Cerebellar Degenerations; Cerebellar Ataxia, Marie; Cerebellar Ataxia, Marie's; Cerebellar Degeneration, Primary; Corticostriatal-Spinal Degenerations; Degeneration, Corticostriatal-Spinal; Degeneration, Familial Spinocerebellar; Degeneration, Hereditary Spinocerebellar; Degeneration, Inherited Spinocerebellar; Degeneration, Primary Cerebellar; Degeneration, Spino Cerebellar; Degeneration, Spino-Cerebellar; Degeneration, Spinocerebellar; Degenerations, Corticostriatal-Spinal; Degenerations, Familial Spinocerebellar; Degenerations, Hereditary Spinocerebellar; Degenerations, Inherited Spinocerebellar; Degenerations, Primary Cerebellar; Degenerations, Spino Cerebellar; Degenerations, Spinocerebellar; Familial Spinocerebellar Degeneration; Garland Moorhouse Syndrome; Hereditary Oligophrenic Cerebello Lental Degeneration; Hereditary Spinocerebellar Degeneration; Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic; Inherited Spinocerebellar Degeneration; Marinesco Garland Syndrome; Marinesco Sjogren Garland Syndrome; Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism; Marinesco Sjogren Syndrome Myopathy; Marinesco Sjögren Syndrome; Primary Cerebellar Degeneration; Primary Cerebellar Degenerations; Spino Cerebellar Degeneration; Spino-Cerebellar Degeneration; Spinocerebellar Degeneration, Familial; Spinocerebellar Degeneration, Hereditary; Spinocerebellar Degeneration, Inherited; Spinocerebellar Degenerations, Familial; Spinocerebellar Degenerations, Hereditary; Spinocerebellar Degenerations, Inherited; Syndrome, Garland-Moorhouse; Syndrome, Marinesco-Garland; Syndrome, Marinesco-Sjogren-Garland; Syndrome, Marinesco-Sjögren; Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren; Syndrome-Myopathy, Marinesco-Sjogren; Ataxias, Hereditary; Cerebellar Ataxia, Early Onset; Cerebellar Ataxia, Late Onset; Cerebellar Degenerations, Primary; Corticostriatal-Spinal Degeneration; Marie Cerebellar Ataxia; Marinesco-Sjogren Syndrome

Nervous System Diseases: 14737
- Neurodegenerative Diseases: 44095
  - Nervous System Heredodegenerative Disorders: 62
    - Spinocerebellar Degenerations: 355
- Central Nervous System Diseases: 4371
  - Brain Diseases: 16141
    - Cerebellar Diseases: 647
      - Spinocerebellar Degenerations: 355
  - Spinal Cord Diseases: 4420
    - Spinocerebellar Degenerations: 355
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Nervous System Heredodegenerative Disorders: 62
    - Spinocerebellar Degenerations: 355

Martin Wendlandt Selected Research

Martin Wendlandt Research Topics

Disease

Drug/Important Bio-Agent (IBA)