Newborn with aplasia cutis caused by epidermolysis bullosa

Autor: Cramer, C., Bay, B., Anne-Bine Skytte, Lauritzen, K. F., Sommerlund, M.

Publikováno v: Cramer, C, Bay, B, Skytte, A-B, Lauritzen, K F & Sommerlund, M 2018, ' Nyfødt med aplasia cutis forårsaget af epidermolysis bullosa ', Ugeskrift for Læger, bind 180, nr. 40 .
Scopus-Elsevier

Epidermiolysis bullosa (EB) is a rare group of genetic disorders, which are characterised by bullae and erosions on skin and mucosa. This case report describes a patient, who was born at full term without any complications. Both crurae were affected

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1b4e68dfb560a85e0e8822389b694e71
https://pure.au.dk/portal/da/publications/nyfoedt-med-aplasia-cutis-foraarsaget-af-epidermolysis-bullosa(1d9b5d36-cb72-403c-8aa6-ef68cb71df0b).html