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Multi-Gene Next-Generation Sequencing for Molecular Diagnosis of Autosomal Recessive Congenital Ichthyosis: A Genotype-Phenotype Study of Four Italian Patients.
Fioretti, Tiziana; Auricchio, Luigi; Piccirillo, Angelo; Vitiello, Giuseppina; Ambrosio, Adelaide; Cattaneo, Fabio; Ammendola, Rosario; Esposito, Gabriella.
Afiliación
  • Fioretti T; CEINGE-Advanced Biotechnologies s.c. a r.l., Via Gaetano Salvatore, 80145 Naples, Italy.
  • Auricchio L; Department of Clinical Medicine and Surgery, University of Naples Federico II, Via S. Pansini, 5, 80131 Naples, Italy.
  • Piccirillo A; San Carlo Hospital, Operating Unit of Dermatology, 85100 Potenza, Italy.
  • Vitiello G; Complex Operating Unit of Medical Genetics, University Hospital Federico II, Via S. Pansini, 5, 80131 Naples, Italy.
  • Ambrosio A; Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, Via S. Pansini, 5, 80131 Naples, Italy.
  • Cattaneo F; Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, Via S. Pansini, 5, 80131 Naples, Italy.
  • Ammendola R; Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, Via S. Pansini, 5, 80131 Naples, Italy.
  • Esposito G; CEINGE-Advanced Biotechnologies s.c. a r.l., Via Gaetano Salvatore, 80145 Naples, Italy.
Diagnostics (Basel) ; 10(12)2020 Nov 24.
Article en En | MEDLINE | ID: mdl-33255364
Autosomal recessive congenital ichthyoses (ARCI) are rare genodermatosis disorders characterized by phenotypic and genetic heterogeneity. At least fourteen genes so far have been related to ARCI; however, despite genetic heterogeneity, phenotypes associated with mutation of different ARCI genes may overlap, thereby making difficult their clinical and molecular classification. In addition, molecular tests for diagnosis of such an extremely rare heterogeneous inherited disease are not easily available in clinical settings. In the attempt of identifying the genetic cause of the disease in four Italian patients with ARCI, we performed next-generation sequencing (NGS) analysis targeting 4811 genes that have been previously linked to human genetic diseases; we focused our analysis on the 13 known ARCI genes comprised in the panel. Nine different variants including three novel small nucleotide changes and two novel large deletions have been identified and validated in the ABCA12, ALOX12B, CYP4F22, and SULT2B1 genes. Notably, two patients had variants in more than one gene. The identification and validation of new pathogenic ABCA12, ALOX12B, CYP4F22, and SULT2B1 variants through multi-gene NGS in four cases of ARCI further highlight the importance of these genes in proper skin function and development.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Diagnostics (Basel) Año: 2020 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Diagnostics (Basel) Año: 2020 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza