Unusual Severe Seborrheic Dermatitis in Two Siblings with Autosomal Recessive Chronic Granulomatous Disease
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To the Editor
We thank our patient and his family for their participation in this study. We thank Instituto PENSI for administrative support.
This work was supported by CAPES to NBZ; The Jeffrey Modell Foundation to ACN; and PENSI Institute and Ministério da Saúde do Brasil (PRONAS/PDC 2015, 25000.077928/2015-6) to ACN.
Compliance with Ethical Standards
Conflict of Interest
The authors declare that they have no conflict of interest.
This study was approved by the Ethics and Research Committee for Humans at the Institute of Biomedical Sciences, University of São Paulo, in accordance with the Declaration of Helsinki. Patients or parents provided written informed consent.
- 4.Vazquez N, Lehrnbecher T, Chen R, Christensen BL, Gallin JI, et al. Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: the significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes. Exp Hematol. 2001;29:234–43.CrossRefGoogle Scholar
- 5.de Oliveira-Junior EB, Zurro NB, Prando C, Cabral-Marques O, Pereira PV, Schimke LF, Klaver S, Buzolin M, Blancas-Galicia L, Santos-Argumedo L, Pietropaolo-Cienfuegos DR, Espinosa-Rosales F, King A, Sorensen R, Porras O, Roxo-Junior P, Forte WC, Orellana JC, Lozano A, GalicchioM, Regairaz L, Grumach AS, Costa-Carvalho BT, Bustamante J, Bezrodnik L, Oleastro M, Danielian S, Condino-Neto. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry. A Pediatr Blood Cancer. 2015;62:2101–7.CrossRefGoogle Scholar