Neuroblastoma Amplified Sequence Gene Mutations Inducing Acute Kidney and Liver Injury in an Adolescent Female
Autor: | Oded Volovelsky, Sheryl L. Johnson, Roy Rafael Dayan, O. N. Ray Bignall, Francisco Flores |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
030232 urology & nephrology Renal function Case Report 030204 cardiovascular system & hematology Gene mutation lcsh:RC870-923 Compound heterozygosity Gastroenterology 03 medical and health sciences 0302 clinical medicine Human genetics Internal medicine medicine Acute tubular necrosis Liver injury Kidney business.industry Acute kidney injury lcsh:Diseases of the genitourinary system. Urology medicine.disease medicine.anatomical_structure Nephrology Liver function business Acute liver failure |
Zdroj: | Case Reports in Nephrology and Dialysis Case Reports in Nephrology and Dialysis, Vol 10, Iss 3, Pp 117-123 (2020) |
ISSN: | 2296-9705 |
Popis: | Acute liver injury (ALI) in children is a life-threatening event, and a definitive etiology can be identified in approximately 50% of cases. Neuroblastoma amplified sequence (NBAS) gene mutations have been associated with a broad phenotypic spectrum of this disease, ranging from recurrent episodes of fever-induced liver injuries to multiorgan involvement, including frequent infections as well as skeletal and immunological abnormalities. Here, we describe an adolescent female with a confirmed compound heterozygous NBAS gene mutation who presented with an episode of ALI complicated by severe acute kidney injury (AKI). The kidney injury was most probably driven by an intrinsic insult, as noted by elevated neutrophil gelatinase-associated lipocalin levels and a kidney biopsy demonstrating severe tubular damage consistent with acute tubular necrosis. While the patient’s liver function and mental status showed significant improvement with supportive care, recovery of kidney function was delayed, and the patient required acute hemodialysis. We suggest a causative relation between the NBAS gene mutation and severe AKI. |
Databáze: | OpenAIRE |
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