info:eu-repo/semantics/article
Urea cycle disorders in Argentine patients: Clinical presentation, biochemical and genetic findings
Fecha
2019-08Registro en:
Silvera Ruiz, Silene Maite; Arranz, José A.; Häberle, Johannes; Angaroni, Celia Juana; Bezard, Miriam; et al.; Urea cycle disorders in Argentine patients: Clinical presentation, biochemical and genetic findings; BioMed Central; Orphanet Journal Of Rare Diseases; 14; 1; 8-2019
1750-1172
CONICET Digital
CONICET
Autor
Silvera Ruiz, Silene Maite
Arranz, José A.
Häberle, Johannes
Angaroni, Celia Juana
Bezard, Miriam
Guelbert, Norberto Bernardo
Becerra, Adriana Berónica
Peralta, Maria Fernanda
Dodelson de Kremer, Raquel
Laróvere, Laura Elena
Resumen
The incidence, prevalence, and molecular epidemiology of urea cycle disorders (UCDs) in Argentina remain underexplored. The present study is the first to thoroughly assess the clinical and molecular profiles of UCD patients examined at a single reference center in Argentina. Forty-nine UCD cases were collected. About half (26/49, 53%) manifested neonatally with classical presentation and had a high mortality (25/26, 96%). Ornithine transcarbamylase deficiency (OTCD) was the most common UCD (26 patients). Argininosuccinate synthetase deficiency (ASSD) was detected in 19 cases, while argininosuccinate lyase deficiency (ASLD) was diagnosed in 4 cases. Molecular genetic analysis revealed 8 private OTC mutations and two large deletion/duplication events in the OTC gene. Most mutations in the ASS1 and ASL genes were recurrent missense changes, and four alterations were novel. The clinical outcome of our UCD cohort was poor, with an overall mortality of 57% (28/49 cases), and a 28% (6/21) disability rate among the survivors. Most patients in our case series showed severe neonatal onset, with high morbidity/ mortality. We detected in total 19 mutations, most of them recurrent and of high frequency worldwide. Noteworthy, we highlight the presence of a geographic cluster with high prevalence of a point mutation in the ASS1 gene. This study suggests that these disorders may be more frequent than commonly assumed, and stresses the need for increased awareness amongst health professionals and greater availability of diagnostic tools for accurate identification, earlydiagnosis, and timely treatment.