Organic acidemia
A rare autosomal inherited organic acid disorder caused by mutations in the PCCA and PCCB genes. It results in the accumulation of harmful organic acids in the blood and urine. Signs and symptoms appear in infancy and include vomiting, poor feeding, loss of appetite, hypotonia, and lethargy.
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Recent Cases of Organic acidemia
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Senior Resident
St Jude Children's Hospital
Research Fellow
Johns Hopkins Hospital
Post doctoral fellow - Pediatric Neuroradiology
Pgimer
M.D (Pediatrics)
New Swasthya Sadan Hospital
Consultant Pediatrician
B.j.medical College
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