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J Pediatr Endocrinol Metab ; 36(8): 782-785, 2023 Aug 28.
Article in English | MEDLINE | ID: mdl-37307239

ABSTRACT

OBJECTIVES: To present a case of a new pathogenic variant of DICER1. CASE PRESENTATION: 13-year-old female with non-toxic multinodular goiter and ovarian Sertoli-Leydig cell tumor, in whom a pineal parenchymal tumor of intermediate differentiation was diagnosed. Next-generation sequencing revealed a new germline mutation in the DICER1 gene (exon 16, c2488del [pGlu830Serfs*2] in heterozygosis), establishing the diagnosis of DICER1 syndrome. CONCLUSIONS: Mutations in the DICER1 gene cause genetic predisposition to a wide spectrum of benign or malignant tumors from childhood to adulthood.


Subject(s)
Brain Neoplasms , Goiter , Ovarian Neoplasms , Pineal Gland , Pinealoma , Sertoli-Leydig Cell Tumor , Male , Female , Humans , Adolescent , Child , Young Adult , Sertoli-Leydig Cell Tumor/genetics , Sertoli-Leydig Cell Tumor/pathology , Ovarian Neoplasms/genetics , Ovarian Neoplasms/pathology , Pineal Gland/pathology , Cell Differentiation/genetics , Ribonuclease III/genetics , DEAD-box RNA Helicases/genetics
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