Abstract

PA and MAA have numerous nonspecific presentations, potentially leading to delayed diagnosis or misdiagnosis. In this paper, we present the clinical and biochemical characteristics of MMA and PA patients at initial presentation. Results. This is a retrospective review of 20 patients with PA (n = 10) and MMA (n = 10). The most observed symptoms were vomiting (85%) and refusing feeding (70%). Ammonia was 108.75 ± 9.3 μmol/l, showing a negative correlation with pH and bicarbonate and positive correlation with lactate and anion gap. Peak ammonia did not correlate with age of onset (r = 0.11 and p = 0.64) or age at diagnosis (r = 0.39 and p = 0.089), nor did pH (r = 0.01, p = 0.96; r = −0.25, p = 0.28) or bicarbonate (r = 0.07, p = 0.76; r = −0.22, p = 0.34). There was no correlation between ammonia and C3 : C2 (r = 0.1 and p = 0.96) or C3 (r = 0.23 and p = 0.32). The glycine was 386 ± 167.1 μmol/l, and it was higher in PA (p = 0.003). There was a positive correlation between glycine and both pH (r = 0.56 and p = 0.01) and HCO3 (r = 0.49 and p = 0.026). There was no correlation between glycine and ammonia (r = −0.435 and p = 0.055) or lactate (r = 0.32 and p = 0.160). Conclusion. Clinical presentation of PA and MMA is nonspecific, though vomiting and refusing feeding are potential markers of decompensation. Blood gas, lactate, and ammonia levels are also good predictors of decompensation, though increasing levels of glycine may not indicate metabolic instability.

Highlights

  • Propionic acidemia (PA) and methylmalonic acidemia (MMA) are autosomal recessive diseases

  • Patients were diagnosed by selective screening prompted by positive family history or suspicious preliminary investigations and clinical presentation

  • All patients were of a Middle Eastern background and born at term (m = 38:6 ± 2:18); 80% had a history of consanguinity, and 45% were females

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Summary

Introduction

Propionic acidemia (PA) and methylmalonic acidemia (MMA) are autosomal recessive diseases They are caused by a defect in propionyl-CoA carboxylase and methylmalonylCoA enzymes, respectively. They present classically in an “early-onset” neonatal acute life-threatening form, including lethargy, vomiting, shock, dehydration, metabolic acidosis, and hyperammonemia. While more common in early onset, both suffer from acute decompensation episodes throughout the course of the illness. These episodes are usually triggered by infection, fasting, fever, or any other stress condition [1, 2]

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