Skip to main content

Medical Subject Headings

Search from vocabulary

Content language

Concept information

... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Nervous System Malformations > Malformations of Cortical Development > Malformations of Cortical Development, Group I > Hippocampal Sclerosis
Nervous System Diseases > Nervous System Malformations > Malformations of Cortical Development > Malformations of Cortical Development, Group I > Hippocampal Sclerosis

Preferred term

Hippocampal Sclerosis  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Ammon Horn Scleroses
  • Ammon Horn Sclerosis
  • Horn Sclerosis, Ammon
  • Sclerosis, Ammon Horn

Scope note

  • Neuronal loss in the hippocampal regions of CA1 and CA4 and less severely CA2 and CA3. Additional loss of hippocampal stratum radiatum, hippocampal atrophy and ASTROGLIOSIS are common. Hippocampal sclerosis is associated with intractable TEMPORAL LOBE EPILEPSY.

History note

  • 2023

In other languages

URI

http://www.yso.fi/onto/mesh/D000092223

Download this concept:

RDF/XML TURTLE JSON-LD Created 7/8/22, last modified 4/26/23