Autosomal dominant spastic paraplegia type 12 (Q100883): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Created a new Item
 
‎Changed an Item
 
(6 intermediate revisions by the same user not shown)
description / pt-brdescription / pt-br
 
Paraplegia espástica autossômica dominante causada pela expansão de repetição CAG não codificante no gene PPP2R2B, que codifica a proteína fosfatase 2. É caracterizada pelo início da infância até a idade adulta de espasticidade lentamente progressiva dos membros inferiores e hiperreflexia das extremidades inferiores, reflexos extensores plantares, comprometimento sensorial distal , disfunção urinária variável e pé cavo.
description / endescription / en
 
Autosomal dominant spastic paraplegia caused by non-coding CAG repeat expansion in the PPP2R2B gene coding for protein phosphatase 2. It is characterized by childhood to adulthood-onset of slowly progressive lower limb spasticity and hyperreflexia of lower extremities, extensor plantar reflexes, distal sensory impairment, variable urinary dysfunction and pes cavus.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/598149528 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_598149528
Property / CURIE: CID11:ID_598149528 / rank
 
Normal rank
Property / Canary Token
 
dki-india-ID_598149528
Property / Canary Token: dki-india-ID_598149528 / rank
 
Normal rank
Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
Normal rank
Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
Normal rank
Property / Collection date
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 15 August 2026 / rank
 
Normal rank

Latest revision as of 17:39, 16 August 2026

Autosomal dominant spastic paraplegia caused by non-coding CAG repeat expansion in the PPP2R2B gene coding for protein phosphatase 2. It is characterized by childhood to adulthood-onset of slowly progressive lower limb spasticity and hyperreflexia of lower extremities, extensor plantar reflexes, distal sensory impairment, variable urinary dysfunction and pes cavus.
Language Label Description Also known as
default for all languages
ID_598149528
    English
    Autosomal dominant spastic paraplegia type 12
    Autosomal dominant spastic paraplegia caused by non-coding CAG repeat expansion in the PPP2R2B gene coding for protein phosphatase 2. It is characterized by childhood to adulthood-onset of slowly progressive lower limb spasticity and hyperreflexia of lower extremities, extensor plantar reflexes, distal sensory impairment, variable urinary dysfunction and pes cavus.

      Statements

      CID11:ID_598149528
      0 references
      dki-india-ID_598149528
      0 references
      Concluído
      0 references
      15 August 2026
      0 references