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JOURNAL OF PEDIATRIC CRITICAL CARE
2016
JOURNAL OF PEDIATRIC CRITICAL CARE
Acute intermittent porphyria is an inherited metabolic disease due to de ciency of the enzyme porphobilinogen deaminase that can affect the autonomic, peripheral and central nervous system. We report an 8 year old female who had presented with hyponatremia, psychiatric manifestations, seizures, hypertension and Posterior Reversible Encephalopathy Syndrome (PRES) with a delayed diagnosis of Acute Intermittent Porphyria. As porphyria is thought to be very rare in pre-pubertal age, in view of the
doi:10.21304/2016.0302.00120
fatcat:5ahu4uqjyrarthvtmttmtjjl2a