Importance about use of high-throughput sequencing in pediatric: case report of a patient with Fanconi-Bickel syndrome

• Autores: Abarca-Barriga, HH, Laso-Salazar, MC, Orihuela-Tacuri, D, Chirinos-Saire, J, Venero-Nuñez, A
• Formato: artículo
• Fecha de Publicación: 2024
• Institución: Instituto Nacional de Enfermedades Neoplásicas
• Repositorio: INEN-Institucional
• Lenguaje: inglés
• OAI Identifier: oai:repositorio.inen.sld.pe:20.500.14703/366
• Enlace del recurso: https: //doi.org/10.1186/s12887-024-04641-1; https://hdl.handle.net/20.500.14703/366
• Nivel de acceso: acceso abierto
• Materia: Exome sequencing; Glycogen storage disease; Hypophosphatemia; Renal tubular acidosis; SLC2A2; https://purl.org/pe-repo/ocde/ford#3.02.21

Background: Fanconi-Bickel syndrome is characterized by hepatorenal disease caused by anomalous glycogen storage. It occurs due to variants in the SLC2A2 gene. We present a male patient of 2 years 7 months old, with failure to thrive, hepatomegaly, metabolic acidosis, hypophosphatemia, hypokalemia, hyperlactatemia. Results: Exome sequencing identified the homozygous pathogenic variant NM_000340.2(SLC2A2):c.1093 C > T (p.Arg365Ter), related with Fanconi-Bickel syndrome. He received treatment with bicarbonate, amlodipine, sodium citrate and citric acid solution, enalapril, alendronate and zolendronate, and nutritional management with uncooked cornstarch, resulting in an improvement of one standard deviation in weight and height. Conclusions: The importance of knowing the etiology in rare genetic disease is essential, not only to determine individual and familial recurrence risk, but also to establish the treatment and prognosis; in this sense, access to a new genomic technology in low- and middle-income countries is essential to shorten the diagnostic odyssey.