[Acute encephalopathy induced by vaccination in an infant with methylmalonic aciduria cblA]

Yupeng Liu1, Tongfei Wu, Haijun Wang

  • 1Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.

Insights

Acute encephalopathy in an infant with methylmalonic aciduria cblA was triggered by routine vaccinations. Early metabolic studies are crucial for diagnosing underlying conditions and improving outcomes in infants experiencing adverse events post-vaccination.

Area of Science:

  • Pediatrics
  • Neurology
  • Metabolic Disorders

Background:

  • Methylmalonic aciduria (cblA type) is a rare inherited metabolic disorder.
  • Vaccination is a critical component of infant healthcare, but rare adverse events can occur.

Observation:

  • A previously healthy 7-month-old boy experienced vomiting and coma shortly after hepatitis B vaccination.
  • A subsequent DTaP vaccination at 15 months precipitated another episode of vomiting, lethargy, and coma.

Findings:

  • Metabolic investigations revealed elevated propionylcarnitine and significantly increased urinary methylmalonic acid, consistent with isolated methylmalonic aciduria.
  • Genetic analysis identified two novel mutations in the MMAA gene, confirming the diagnosis of cblA type methylmalonic aciduria.
  • The patient showed significant clinical and biochemical improvement following hydroxylcobalamin treatment, dietary modifications, and L-carnitine supplementation.

Implications:

  • This case highlights the first documented instance of vaccination-induced acute encephalopathy in an infant with methylmalonic aciduria cblA in China.
  • It underscores the importance of considering metabolic disorders in infants presenting with neurological symptoms post-vaccination.
  • Prompt metabolic evaluation and appropriate management are essential for improving outcomes in affected children.
Abstract

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