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Three-country snapshot of ornithine transcarbamylase deficiency

Authors :
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
Seker Yilmaz B., Baruteau J., ARSLAN N., AYDIN H. İ. , Barth M., Bozaci A. E. , Brassier A., CANDA E., Cano A., Chronopoulou E., et al.
Source :
Life; Volume 12; Issue 11; Pages: 1721
Publication Year :
2022

Abstract

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.<br />Medical Research Council [MR/S019111/1]; National Institute of Health Research Senior Investigator Award [NIHR202370]; Medical Research Council Clinician Scientist Fellowship [MR/T008024/1]; NIHR Great Ormond Street Hospital Biomedical Research Centre<br />This work was supported by the Medical Research Council grant, reference: MR/S019111/1. PG is supported by a National Institute of Health Research Senior Investigator Award (Reference NIHR202370). J.B. is supported by Medical Research Council Clinician Scientist Fellowship MR/T008024/1 and NIHR Great Ormond Street Hospital Biomedical Research Centre. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health.

Details

Language :
English
Database :
OpenAIRE
Journal :
Life; Volume 12; Issue 11; Pages: 1721
Accession number :
edsair.doi.dedup.....5258f069f22ac0dff6b3f3ca01169341