Symptomatic form of Becker muscular dystrophy in female carriers (Q93404): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed label, description and/or aliases in pt-br, en
‎Changed an Item
 
(5 intermediate revisions by the same user not shown)
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/853926582 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_853926582
Property / CURIE: CID11:ID_853926582 / rank
 
Normal rank
Property / Canary Token
 
dki-india-ID_853926582
Property / Canary Token: dki-india-ID_853926582 / 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 08:30, 16 August 2026

Becker muscular dystrophy (BMD) in females carriers are characterised by variable degrees of muscle weakness due to progressive skeletal myopathy, sometimes associated with dilated cardiomyopathy or left ventricle dilation. Prevalence is unknown: Only a small percentage of female carriers have been reported to manifest these diseases (19% of female carriers from families with BMD). Symptomatic female carriers usually present later in life. Females with clinical features of BMD are usually carriers of X-chromosome rearrangements, display skewed X-inactivation or have Turner syndrome (complete or partial absence of an X chromosome). The prognosis for symptomatic female carriers is variable, but the disease course tends to be milder in females than in males and progression is slow.
Language Label Description Also known as
default for all languages
ID_853926582
    English
    Symptomatic form of Becker muscular dystrophy in female carriers
    Becker muscular dystrophy (BMD) in females carriers are characterised by variable degrees of muscle weakness due to progressive skeletal myopathy, sometimes associated with dilated cardiomyopathy or left ventricle dilation. Prevalence is unknown: Only a small percentage of female carriers have been reported to manifest these diseases (19% of female carriers from families with BMD). Symptomatic female carriers usually present later in life. Females with clinical features of BMD are usually carriers of X-chromosome rearrangements, display skewed X-inactivation or have Turner syndrome (complete or partial absence of an X chromosome). The prognosis for symptomatic female carriers is variable, but the disease course tends to be milder in females than in males and progression is slow.

      Statements

      CID11:ID_853926582
      0 references
      dki-india-ID_853926582
      0 references
      Concluído
      0 references
      15 August 2026
      0 references