Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: A case of Omenn syndrome

Edwin Cuperus; Joris M. van Montfrans; Mariëlle E. van Gijn; Maarten T. Bastiaens; Mirjam M.A. de Willigen; Roos J. Leguit; Carla A.F.M.  Bruijnzeel-Koomen; Ingrid M.B.  Russel-Kampschoer; Suzanne G.M.A. Pasmans

doi:10.1684/ejd.2017.2992

Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: A case of Omenn syndrome

Edwin Cuperus
, Joris M. van Montfrans
, Mariëlle E. van Gijn
, Maarten T. Bastiaens
, Mirjam M.A. de Willigen
, Roos J. Leguit
, Carla A.F.M. Bruijnzeel-Koomen
, Ingrid M.B. Russel-Kampschoer
, Suzanne G.M.A. Pasmans

Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

Original language	English
Pages (from-to)	313-314
Number of pages	2
Journal	European Journal of Dermatology
Volume	27
Issue number	3
DOIs	https://doi.org/10.1684/ejd.2017.2992
Publication status	Published - 1 May 2017

Access to Document

10.1684/ejd.2017.2992

Cite this

Cuperus, E., van Montfrans, J. M., van Gijn, M. E., Bastiaens, M. T., de Willigen, M. M. A., Leguit, R. J., Bruijnzeel-Koomen, C. A. F. M., Russel-Kampschoer, I. M. B., & Pasmans, S. G. M. A. (2017). Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: A case of Omenn syndrome. European Journal of Dermatology, 27(3), 313-314. https://doi.org/10.1684/ejd.2017.2992

@article{8ea3241dc9a645bfbfdc14f9c881b774,

title = "Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: A case of Omenn syndrome",

author = "Edwin Cuperus and \{van Montfrans\}, \{Joris M.\} and \{van Gijn\}, \{Mari{\"e}lle E.\} and Bastiaens, \{Maarten T.\} and \{de Willigen\}, \{Mirjam M.A.\} and Leguit, \{Roos J.\} and Bruijnzeel-Koomen, \{Carla A.F.M.\} and Russel-Kampschoer, \{Ingrid M.B.\} and Pasmans, \{Suzanne G.M.A.\}",

year = "2017",

month = may,

day = "1",

doi = "10.1684/ejd.2017.2992",

language = "English",

volume = "27",

pages = "313--314",

journal = "European Journal of Dermatology",

issn = "1167-1122",

publisher = "John Libbey",

number = "3",

}

Cuperus, E, van Montfrans, JM, van Gijn, ME, Bastiaens, MT, de Willigen, MMA, Leguit, RJ, Bruijnzeel-Koomen, CAFM, Russel-Kampschoer, IMB & Pasmans, SGMA 2017, 'Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: A case of Omenn syndrome', European Journal of Dermatology, vol. 27, no. 3, pp. 313-314. https://doi.org/10.1684/ejd.2017.2992

TY - JOUR

T1 - Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency

T2 - A case of Omenn syndrome

AU - Cuperus, Edwin

AU - van Montfrans, Joris M.

AU - van Gijn, Mariëlle E.

AU - Bastiaens, Maarten T.

AU - de Willigen, Mirjam M.A.

AU - Leguit, Roos J.

AU - Bruijnzeel-Koomen, Carla A.F.M.

AU - Russel-Kampschoer, Ingrid M.B.

AU - Pasmans, Suzanne G.M.A.

PY - 2017/5/1

Y1 - 2017/5/1

UR - https://www.scopus.com/pages/publications/85021879411

U2 - 10.1684/ejd.2017.2992

DO - 10.1684/ejd.2017.2992

M3 - Comment/Letter to the editor

C2 - 28414192

AN - SCOPUS:85021879411

SN - 1167-1122

VL - 27

SP - 313

EP - 314

JO - European Journal of Dermatology

JF - European Journal of Dermatology

IS - 3

ER -

Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: A case of Omenn syndrome

Access to Document

Other files and links

Cite this