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4-Hydroxybutyric Aciduria as a Rare Presentation of Global Developmental Delay in Children: Case Report of Two Different Patients
4-Hydroxybutyric Aciduria as a Rare Presentation of Global Developmental Delay in Children: Case Report of Two Different Patients

Rahim Vakili; Mehran Beiraghi Toosi; Asma Javid; Nahid Donyadideh; Farnoosh Ebrahimzadeh; Narges Hashemi; Somayeh Hashemian

Volume 6, Issue 7 , July 2018, , Pages 7861-7865

https://doi.org/10.22038/ijp.2018.27462.2367

Abstract
  Succinic semialdehyde dehydrogenase (SSADH) deficiency or 4-Hydroxybutyric Aciduria is an autosomal recessive inherited disorder of amma-aminobutyric acid (GABA) degradation. It ...  Read More