Life (Oct 2022)

Three-Country Snapshot of Ornithine Transcarbamylase Deficiency

  • Berna Seker Yilmaz,
  • Julien Baruteau,
  • Nur Arslan,
  • Halil Ibrahim Aydin,
  • Magalie Barth,
  • Ayse Ergul Bozaci,
  • Anais Brassier,
  • Ebru Canda,
  • Aline Cano,
  • Efstathia Chronopoulou,
  • Grainne M. Connolly,
  • Lena Damaj,
  • Charlotte Dawson,
  • Dries Dobbelaere,
  • Claire Douillard,
  • Fatma Tuba Eminoglu,
  • Sahin Erdol,
  • Melike Ersoy,
  • Sherry Fang,
  • François Feillet,
  • Gulden Gokcay,
  • Emine Goksoy,
  • Magali Gorce,
  • Asli Inci,
  • Banu Kadioglu,
  • Fatih Kardas,
  • Cigdem Seher Kasapkara,
  • Gonca Kilic Yildirim,
  • Deniz Kor,
  • Melis Kose,
  • Cecilia Marelli,
  • Helen Mundy,
  • Siobhan O’Sullivan,
  • Burcu Ozturk Hismi,
  • Radha Ramachandran,
  • Agathe Roubertie,
  • Mehtap Sanlilar,
  • Manuel Schiff,
  • Srividya Sreekantam,
  • Karolina M. Stepien,
  • Ozlem Uzun Unal,
  • Yilmaz Yildiz,
  • Tanyel Zubarioglu,
  • Paul Gissen

DOI
https://doi.org/10.3390/life12111721
Journal volume & issue
Vol. 12, no. 11
p. 1721

Abstract

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X-linked ornithine transcarbamylase deficiency (OTCD) is the most common urea cycle defect. The disease severity ranges from asymptomatic carrier state to severe neonatal presentation with hyperammonaemic encephalopathy. We audited the diagnosis and management of OTCD, using an online 12-question-survey that was sent to 75 metabolic centres in Turkey, France and the UK. Thirty-nine centres responded and 495 patients were reported in total. A total of 208 French patients were reported, including 71 (34%) males, 86 (41%) symptomatic and 51 (25%) asymptomatic females. Eighty-five Turkish patients included 32 (38%) males, 39 (46%) symptomatic and 14 (16%) asymptomatic females. Out of the 202 UK patients, 66 (33%) were male, 83 (41%) asymptomatic and 53 (26%) symptomatic females. A total of 19%, 12% and 7% of the patients presented with a neonatal-onset phenotype in France, Turkey and the UK, respectively. Vomiting, altered mental status and encephalopathy were the most common initial symptoms in all three countries. While 69% in France and 79% in Turkey were receiving protein restriction, 42% were on a protein-restricted diet in the UK. A total of 76%, 47% and 33% of patients were treated with ammonia scavengers in Turkey, France and the UK, respectively. The findings of our audit emphasize the differences and similarities in manifestations and management practices in three countries.

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