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Updated: May 15, 2026

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
Lethal Netherton syndrome due to homozygous p.Arg371X mutation in SPINK5
Andrea Diociaiuti1, Daniele Castiglia, Paola Fortugno
1Dermatology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy. andrea.diociaiuti@tin.it
Abstract:
Here we report a lethal case of Netherton syndrome presenting with neurologic complications, hypernatremic dehydration, failure to thrive, and episodes of sepsis. Molecular analysis of the serine protease inhibitor Kazal-type 5 gene identified a homozygous mutation (c.1111C>T, p.Arg371X). This case highlights the importance of early diagnosis to start appropriate care in a timely fashion and prevent disease complications.
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