Skin manifestations among GATA2-deficient patients.

Polat, A; Dinulescu, M; Fraitag, S; Nimubona, S; Toutain, F; Jouneau, S; Poullot, E; Droitcourt, C; Dupuy, A

Polat, A; Dinulescu, M; Fraitag, S; Nimubona, S; Toutain, F; Jouneau, S; Poullot, E; Droitcourt, C; Dupuy, A.

Affiliation

Polat A; Dermatology Department, CHU Rennes, Rennes, France.
Dinulescu M; Dermatology Department, CHU Rennes, Rennes, France.
Fraitag S; Pathology Department, Hôpital Necker-Enfants Malades, APHP, Paris, France.
Nimubona S; Haematology Department, CHU Rennes, Rennes, France.
Toutain F; Pediatric Department, CHU Rennes, Rennes, France.
Jouneau S; Respiratory Department, CHU Rennes, Rennes, France.
Poullot E; IRSET UMR 1085, Rennes 1 University, Rennes, France.
Droitcourt C; Pathology Department, CHU Rennes, Rennes, France.
Dupuy A; Dermatology Department, CHU Rennes, Rennes, France.

Br J Dermatol ; 178(3): 781-785, 2018 03.

Article in En | MEDLINE | ID: mdl-28440875

Subject(s)

GATA2 Deficiency/complications; GATA2 Transcription Factor/genetics; Mutation/genetics; Skin Diseases/genetics; Adult; Child; Erythema Nodosum/genetics; Facial Dermatoses/genetics; Female; GATA2 Deficiency/diagnosis; Gingival Hypertrophy/genetics; Glossitis/genetics; Humans; Lupus Erythematosus, Cutaneous/genetics; Lymphedema/genetics; Male; Young Adult

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Diseases / GATA2 Transcription Factor / GATA2 Deficiency / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Child / Female / Humans / Male Language: En Journal: Br J Dermatol Year: 2018 Type: Article Affiliation country: France

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