Hereditary orotic aciduria with epilepsy and without megaloblastic anemia

Neuropediatrics

Volumn 46, Issue 2, 2015, Pages 123-125

  Grohmann, Karina ^a,b   Lauffer, Heinz ^a   Lauenstein, Peter ^a   Hoffmann, Georg F ^b   Seidlitz, Günter ^a  

^a UNIVERSITY MEDICINE GREIFSWALD   (Germany)

^b UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

Author keywords

epilepsy; hereditary orotic aciduria; UMPS deficiency

Indexed keywords

OROTIC ACID; OXCARBAZEPINE; UNCLASSIFIED DRUG; URIDINE; URIDINE 5 MONOPHOSPHATE SYNTHASE; URIDINE PHOSPHATE;

ACIDURIA; ARTICLE; ATTENTION DEFICIT DISORDER; CASE REPORT; CHILD; ELECTROENCEPHALOGRAM; EPILEPSY; FOLLOW UP; HEREDITARY OROTIC ACIDURIA; HUMAN; MALE; MEGALOBLASTIC ANEMIA; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRESCHOOL CHILD; PRIORITY JOURNAL; RESTLESSNESS; SCHOOL CHILD; SEIZURE; TONIC CLONIC SEIZURE; URINARY EXCRETION;

EID: 84964255444     PISSN: 0174304X     EISSN: 14391899     Source Type: Journal    
DOI: 10.1055/s-0035-1547341     Document Type: Article

References (6)

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