Netherton syndrome caused by compound heterozygous mutation, c.80A > G mutation in SPINK5 and large ‐sized genomic deletion mutation, and successful treatment of intravenous immunoglobulin

ConclusionsThis is the first observation of NS caused by a large deletion. Our findings have important implications for mutation screening and genetic counseling in NS. Our report also verifies and supports the safety and efficacy of IVIG therapy in patients with NS.

Source: Molecular Genetics & Genomic Medicine - January 16, 2021 Category: Genetics & Stem Cells Authors: Zhen Zhang, Chaolan Pan, Ruoqu Wei, Huaguo Li, Yijun Yang, Jiawen Chen, Ming Li, Zhirong Yao Tags: ORIGINAL ARTICLE Source Type: research