• Amanda M Narcizo, Lais C Cardoso, Anna F F Benedetti, Alexander A L Jorge, Mariana F A Funari, Barbara L Braga, Monica M Franca, Luciana R Montenegro, Antonio M Lerario, Mirian Y Nishi, and Berenice B Mendonca.
• Laboratório de Sequenciamento em Larga Escala (SELA), Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil. Electronic address: amnarcizo@usp.br.
• Clinics (Sao Paulo). 2022 Jan 1; 77: 100132100132.

ObjectivesTo analyze the efficiency of a multigenic targeted massively parallel sequencing panel related to endocrine disorders for molecular diagnosis of patients assisted in a tertiary hospital involved in the training of medical faculty.Material And MethodsRetrospective analysis of the clinical diagnosis and genotype obtained from 272 patients in the Endocrine unit of a tertiary hospital was performed using a custom panel designed with 653 genes, most of them already associated with the phenotype (OMIM) and some candidate genes that englobes developmental, metabolic and adrenal diseases. The enriched DNA libraries were sequenced in NextSeq 500. Variants found were then classified according to ACMG/AMP criteria, with Varsome and InterVar.ResultsThree runs were performed; the mean coverage depth of the targeted regions in panel sequencing data was 249×, with at least 96.3% of the sequenced bases being covered more than 20-fold. The authors identified 66 LP/P variants (24%) and 27 VUS (10%). Considering the solved cases, 49 have developmental diseases, 12 have metabolic and 5 have adrenal diseases.ConclusionThe application of a multigenic panel aids the training of medical faculty in an academic hospital by showing the picture of the molecular pathways behind each disorder. This may be particularly helpful in developmental disease cases. A precise genetic etiology provides an improvement in understanding the disease, guides decisions about prevention or treatment, and allows genetic counseling.Copyright © 2022 HCFMUSP. Published by Elsevier España, S.L.U. All rights reserved.

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