| Summary: | 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 <i>ABCA12</i>, <i>ALOX12B</i>, <i>CYP4F22</i>, and <i>SULT2B1</i> genes. Notably, two patients had variants in more than one gene. The identification and validation of new pathogenic <i>ABCA12</i>, <i>ALOX12B</i>, <i>CYP4F22</i>, and <i>SULT2B1</i> 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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