| Revue: | Genetics and molecular biology |
| Base de datos: | PERIÓDICA |
| Número de sistema: | 000459242 |
| ISSN: | 1415-4757 |
| Autores: | Wang, Wenda1 Zhao, Yang1 Wang, Xu1 Wang, Zhan1 Cai, Yi2 Li, Hanzhong1 Zhang, Yushi1 |
| Instituciones: | 1Chinese Academy of Sciences, Peking Union Medical College Hospital, Beijing. China 2Central South University, Xiangya Hospital, Changsha, Hunan. China |
| Año: | 2022 |
| Volumen: | 45 |
| Número: | 2 |
| País: | Brasil |
| Idioma: | Inglés |
| Tipo de documento: | Artículo |
| Enfoque: | Analítico |
| Resumen en inglés | We sought to explore the relationship between renal lesion features and genetic mutations in tuberous sclerosis complex (TSC) patients. TSC patients with renal lesions were subjected to TSC1/2 gene next-generation sequencing (NGS). TSC1/2 mutation types and imaging examinations were screened for combined analysis of genetic and clinical features. Seventy-three probands among TSC patients with renal lesions were included. Twenty affected relatives were also included. In total, 93 patients were included. Eighty patients (86.0%) had bilateral renal angiomyolipomas (AMLs), and one had epithelioid AML. Two patients had polycystic kidney disease, one had renal cell carcinoma, and one had Wilms tumor. Among the 73 probands, four had TSC1 mutations, 53 had TSC2 mutations, and 16 had no mutations identified (NMI). There was no statistically significant difference between TSC1 mutation, TSC2 mutation and NMI group (P= 0.309), or between familial and sporadic groups (P= 0.775) when considering AML size. There was no statistically significant difference between pathogenic/likely pathogenic and benign/likely benign/NMI groups (P= 0.363) or among patients with different mutation types of TSC2 (P= 0.906). The relationship between the conditions of TSC gene mutations and the severity of renal lesions still needs more analysis. Patients with NMI, particularly those with familial disease, need more attention because the pathogenesis remains unknown |
| Disciplinas: | Biología, Medicina |
| Palabras clave: | Genética, Urología, Esclerosis tuberosa, Lesión renal aguda (LRA), Mutaciones, Gen TSC |
| Keyword: | Genetics, Urology, Tuberous sclerosis, Acute renal failure (ARF), Mutations, TSC2 gen |
| Texte intégral: | Texto completo (Ver HTML) Texto completo (Ver PDF) |
