| CASE REPORT
|Year : 2019 | Volume
| Issue : 3 | Page : 133-136
Arginase deficiency presenting as acute encephalopathy
Leema Pauline Cornelius, Vivekasaravanan Raju, Asir Julin
Department of Paediatric Neurology, Institute of Child Health and Hospital for Children, Madras Medical College, Chennai, Tamil Nadu, India
Urea cycle disorders are rare metabolic disorders that present as encephalopathy with hyperammonemia. Arginase deficiency causing hyperargininemia is one among the urea cycle disorders, which usually presents as spastic diplegia. Hyperammonemic encephalopathy is rare in arginase deficiency. We present a rare case of arginase deficiency presenting as acute encephalopathy in a child.
Dr. Leema Pauline Cornelius
Department of Paediatric Neurology, Institute of Child Health and Hospital for Children, Egmore, Chennai, Tamil Nadu.
Source of Support: None, Conflict of Interest: None
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