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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.
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.
Abstract:
Due to the rarity of this disorder, paying attention to diagnostic clues is important. Low valine formula seems to be effective in improvement of patient's symptoms. Prevention of consanguineous marriage is the best way to prevent this disease.
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