Research advances of Netherton syndrome
Netherton syndrome (NS) is a rare recessive syndromic ichthyosis due to mutations in the SPINK5 gene characterized by a triad read more of congenital ichthyosiform erythroderma (CIE) and/or ichthyosis linearis circumflexa (ILC), hair shaft abnormalities, and elevated IgE levels.However, NS patients often suffer from misdiagnosis, delayed treatment,