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Description
Acute hyperammonemia is less frequent, and patients mostly present with progressive spasticity, intellectual disability, and sometimes seizures after the second year of age.3 Organic acidurias (OA) and hyperammonemia OA are all autosomal-recessive inherited disorders mainly affecting branched-chain amino acid degradation
Date : DMF Number : 3314 Submission : 1978-09-12 Status : Inactive Type : II Product Web Link USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others GDUFA DMF Review : N/A Rev
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