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
Hauptverfasser: Bellon, N., Hadj‐Rabia, S., Moulin, F., Lambe, C., Lezmi, G., Charbit‐Henrion, F., Alby, C., Le Saché‐de Peufeilhoux, L., Leclerc‐Mercier, S., Hadchouel, A., Steffann, J., Hovnanian, A., Lapillonne, A., Bodemer, C.
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Sprache:eng
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