Abstract
Netherton syndrome (NS; OMIM 256500), also known as Comel–Netherton syndrome, is a rare but severe autosomal recessive skin disorder first reported by Comel in 1949 and Netherton in 1958. It is cha...
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
