3-Hydroxyisobutyryl-CoA hydrolase deficiency in an infant with developmental delay and high anion gap acidosis

Hedyeh Saneifard1, Asieh Mosallanejad2, Aida Fallahzadeh3,4

  • 1Mofid Children's Hospital Shahid Beheshti University of Medical Sciences Tehran Iran.

Clinical Case Reports
|July 29, 2021
PubMed

Insights

Diagnosing rare disorders requires attention to key clues. A low valine formula can improve patient symptoms, and preventing consanguineous marriage is crucial for disease prevention.

Area of Science:

  • Biochemistry
  • Genetics
  • Metabolic Disorders

Background:

  • Rare genetic disorders present diagnostic challenges.
  • Early identification of specific metabolic pathways is critical for effective management.
  • Understanding the genetic basis of rare diseases informs prevention strategies.

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