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J Pediatr ; 176: 204-6, 2016 09.
Article in English | MEDLINE | ID: mdl-27301573

ABSTRACT

Myeloperoxidase deficiency is the most common inherited phagocyte disorder (1:2000) and causes an abnormal dihydrorhodamine oxidation test, which also is seen in chronic granulomatous disease. A patient with Candida meningitis and low dihydrorhodamine oxidation signal was diagnosed with chronic granulomatous disease but actually had compound heterozygous myeloperoxidase deficiency.


Subject(s)
Granulomatous Disease, Chronic/diagnosis , Metabolism, Inborn Errors/diagnosis , Diagnosis, Differential , False Positive Reactions , Humans , Male , Oxidation-Reduction , Rhodamines/metabolism , Young Adult
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