Hyperammonaemic Encephalopathy Caused by Adult-Onset Ornithine Transcarbamylase Deficiency.
Bjarke Hammer NiclasenMaria Therese Schelde-OlesenMads AstvadAnders LøkkeThomas KrøigårdHelle Hvilsted NielsenPublished in: Brain sciences (2022)
Hyperammonaemic encephalopathy in adults is a rare condition in the absence of liver disease and is associated with a high mortality and risk of permanent neurological deficits. Seldomly, the condition is caused by an inborn error of metabolism in the urea cycle, triggered by an exogenic factor such as gastrointestinal haemorrhage, gastric bypass surgery, starvation, seizures, vigorous exercise, burn injuries, or drugs hampering the elimination of ammonia. Here, we present a fatal case of an unrecognized genetic ornithine transcarbamylase deficiency (OTCD) presenting with a subacute progressive encephalopathy. We review the current literature and discuss the differential diagnosis and treatment options. As swift diagnosis and initiation of treatment is vital, awareness of hyperammonaemic encephalopathy and its possible causes can help improve the prognosis of this condition.
Keyphrases
- early onset
- gastric bypass
- physical activity
- roux en y gastric bypass
- minimally invasive
- multiple sclerosis
- replacement therapy
- systematic review
- weight loss
- obese patients
- high intensity
- type diabetes
- risk factors
- coronary artery disease
- genome wide
- cardiovascular events
- gene expression
- body composition
- acute coronary syndrome
- dna methylation
- atrial fibrillation
- blood brain barrier
- subarachnoid hemorrhage