The challenging management of a series of 43 infants with Netherton syndrome: unexpected complications and novel mutations
Summary Background Netherton syndrome (NS) is a rare disease caused by SPINK5 mutations, featuring variable skin and hair involvement and, in many cases, allergic manifestations with a risk of lethality, particularly in infants. The clinical management of NS is challenging. Objectives To analyse the...
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Veröffentlicht in: | British journal of dermatology (1951) 2021-03, Vol.184 (3), p.532-537 |
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Format: | Artikel |
Sprache: | eng |
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