Early detection, lifetime protection: ADA-SCID identification and management, from cradle to adulthood

Early detection, lifetime protection: ADA-SCID identification and management, from cradle to adulthood

In this online, self-learning activity: Adenosine deaminase-deficient severe combined immunodeficiency (ADA-SCID) is a rare genetic disorder caused by mutations in the adenosine deaminase (ADA) gene. ADA-SCID is a specific form of severe combined immunodeficiency that results from ADA deficiency. Mutations in the ADA gene result in an accumulation of deoxyadenosine which leads to the destruction of lymphocytes, affecting the integrity of the immune system. This disease leaves individuals highly susceptible to infection such as pneumonia, chronic diarrhea, and oral thrush, which typically manifests soon after birth. The median age at diagnosis is between 1-3 months of age, although there is variability with some individuals having a later presentation onset. ADA deficiency accounts for approximately 10-15% of all SCID cases with an overall prevalence of 1 in 500,000 live births. It remains a rare disease and requires specialized immunologists, novel gene therapies, and transplant physicians to create a wholistic care plan.

  • Provider:ScientiaCME
  • Activity Link: https://www.scientiacme.org/cme
  • Start Date: 2025-02-15 06:00:00
  • End Date: 2025-02-15 06:00:00
  • Credit Details: AMA PRA Category 1 Credit™️: 1.0 hours
  • MOC Credit Details: ABP - 1.0 Point; Credit Type(s): Lifelong Learning and Self-Assessment (ABP)
  • Commercial Support: Source: Chiesi - Amount: 51895.0 - Is Kind Support: False
  • Activity Type: Enduring Material
  • CME Finder Type: Online Learning
  • Fee to Participate: No, it's free
  • Measured Outcome: Learner Competence, Learner Knowledge, Learner Performance
  • Provider Ship: Directly Provided
  • Registration: Open to all
  • Specialty: Pediatric Infectious Diseases
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