Propionic acidemia is a rare metabolic disorder that affects the catabolism of branched-chain amino acids and oddchain fatty acids. Propionic acidemia is one of the least common organic acidemias.

Propionic acidemia is an inherited disorder caused by deficiency of propionyl-CoA carboxylase. Although it is one of the most frequent organic acidurias, information on the outcome of affected ...

Kerala doctors successfully performed a life-saving liver transplant on a two-and-a-half-year-old child diagnosed with the ...

Here we describe a 6-year-old Thai boy with PA who was born to consanguineous parents. The first three children of this family died in infancy owing to metabolic acidosis, but without a definite ...

Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, China Background: Propionic acidemia (PA) is an inherited autosomal recessive metabolic disorder ...

Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan. Division of Cardiovascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan. Propionic ...

Faculty of Medicine, Pharmacy, and Dentistry, Albert Royer National Children’s Hospital, Cheikh Anta Diop University of Dakar, Dakar, Senegal. We report a case of neonatal propionic acidemia diagnosed ...

After completing enrollment in 5 dose cohorts, and with no dose-limiting safety signals observed to date by the independent DSMB, the Phase 1/2 trial of mRNA-3927 advances to the dose-expansion phase ...