Journal Article

Ornithine Transcarbamylase Deficiency Presenting with Symptoms of Mania in a Young Adult Male

Pentz, Jonathan, Igboeli, Blessing, Niedermier, Julie

2021

Overview

The purpose of this case study is to review the clinical presentation and medical workup of a young adult male presenting with acute behavior changes in the setting of undiagnosed ornithine transcarbamylase deficiency (OTCD). This case study involves a 19-year-old male with a psychiatric history of depression and one previous suicide attempt, who presented to a large midwestern university hospital emergency department after being found by police naked in a neighbor's yard. He displayed manic signs and symptoms, including euphoria, lack of sleep for five days, and attempting to purchase a new car and three large screen TVs. Family reported the patient uncharacteristically announced three weeks earlier that he was vegetarian and stopped eating his frequent customary cheeseburgers. Due to increased anxiety and inability to sleep, the patient received lorazepam 2 mg in the emergency department. Upon transfer to the psychiatric unit, therapy was initiated with aripiprazole 5 mg daily and valproate 1000 mg nightly on Day 1 of treatment. The patient refused medications on hospital Day 2, then received this combination again on Day 3. The next morning, the patient complained of lethargy, headache, nausea, and vomiting. The patient's ammonia level was found to be 204 micromol/L with ALT and AST of 714 and 647 IU/L respectively. Tests for infectious hepatitis were negative. Medical consultation recommended discontinuation of current medications, vigorous hydration, and further work up. On further investigation, the patient was found to have low plasma citrulline level of 8 micromol/L, undetectable plasma arginine, and high urinary orotic acid. The laboratory data showed a biochemical phenotype consistent with a diagnosis of partial OTCD, an X-linked urea cycle disorder resulting in toxic hyperammonemia. The patient was treated with a low protein diet modification as well as a combination of sodium benzoate and sodium phenylbutyrate to reduce serum ammonia concentration. With treatment the patient's laboratory values normalized, and mental status improved. In conclusion, partial ornithine transcarbamylase deficiency may manifest with psychiatric symptoms in early adulthood. In young patients with elevated ammonia and mental status change, OTCD is an important diagnosis to consider, as it is the most common inherited cause of hyperammonemia.

• Publisher: Cambridge University Press
• Subject: Abstracts / Diet, Protein-Restricted / Emergency medical care / Humans / Hyperammonemia - blood / Hyperammonemia - diet therapy / Hyperammonemia - drug therapy / Hyperammonemia - etiology / Laboratories / Male / Mania - blood / Mania - diet therapy / Mania - drug therapy / Mania - etiology / Ornithine Carbamoyltransferase Deficiency Disease - blood / Ornithine Carbamoyltransferase Deficiency Disease - complications / Ornithine Carbamoyltransferase Deficiency Disease - diet therapy / Ornithine Carbamoyltransferase Deficiency Disease - drug therapy / Phenylbutyrates - therapeutic use / Sodium Benzoate - therapeutic use / Treatment Outcome / Young Adult / Young adults