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Three-country snapshot of ornithine transcarbamylase deficiency
- 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.
- Subjects :
- INVOLVEMENT
MICROBIOLOGY
LIVER
Mikrobiyoloji
Temel Tıp Bilimleri
BIOLOGY
Life Sciences (LIFE)
hyperammonaemia
Sağlık Bilimleri
FREQUENCY
DIAGNOSIS
Fundamental Medical Sciences
Biochemistry
BIOLOGY & BIOCHEMISTRY
General Biochemistry, Genetics and Molecular Biology
Tıbbi Biyoloji
Biyokimya
ornithine transcarbamylase deficiency
neonatal-onset
late-onset
asymptomatic
protein restriction
ammonia scavengers
liver transplantation
Yaşam Bilimleri
Health Sciences
Biyoloji ve Biyokimya
Ecology, Evolution, Behavior and Systematics
Medical Biology
Temel Bilimler
Biochemistry (medical)
GENE-THERAPY
Paleontology
Life Sciences
Biyokimya (tıbbi)
UREA CYCLE DISORDERS
EFFICACY
Tıp
Space and Planetary Science
Yaşam Bilimleri (LIFE)
DISEASES
SAFETY
BİYOLOJİ
Medicine
Natural Sciences
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Life; Volume 12; Issue 11; Pages: 1721
- Accession number :
- edsair.doi.dedup.....5258f069f22ac0dff6b3f3ca01169341