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Function: require_once
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039470 | PMC |
http://dx.doi.org/10.1016/j.ekir.2021.12.040 | DOI Listing |
Int J Health Policy Manag
November 2024
Breast Diseases Research Center (BDRC), Cancer Institute, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
J Dermatol
November 2024
Department of Dermatology, Faculty of Medicine, Oita University, Oita, Japan.
Ital J Pediatr
November 2024
Respiratory Department II, National Clinical Research Center for Respiratory Diseases, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, NO.56, Nanlishi Road, 100045, China.
We present two rare cases of p67phox-deficient chronic granulomatous disease (CGD) caused by compound heterozygous mutations in the NCF2 gene. They developed cervical lymphadenitis as the initial manifestation of CGD but had distinct clinical progressions. Patient 1 presented with aspergillous meningitis, an extremely rare manifestation of neurological involvement in CGD, which has not been reported before.
View Article and Find Full Text PDFInt J Dermatol
October 2024
Meridian Dermatology, Meridian, Idaho, USA.
Asian J Surg
October 2024
Department of Pulmonary and Critical Care Medicine, West China Hospital, Sichuan University, Chengdu, 610041, China; State Key Laboratory of Respiratory Health and Multimorbidity, Chengdu, 610041, China. Electronic address:
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