Clinical manifestations of 42 Moroccan patients with chronic granulomatous disease
Assma Dably, Ibtihal Benhssaein, Jalila El Bakkouri, Asmaa Drissi Bourhanbour, Leila Jeddane, Ahmed Aziz Bousfiha, Fatima Ailal

TL;DR
This study describes the clinical features and outcomes of 42 Moroccan patients with chronic granulomatous disease, highlighting common infections and the need for early diagnosis.
Contribution
The study provides a detailed clinical overview of CGD in a Moroccan cohort, emphasizing local disease patterns and mortality factors.
Findings
Skin infections, pneumonia, and Aspergillus-related complications were the most common clinical manifestations.
Aspergillosis was the primary cause of death among the 17 patients who died.
BCGitis and inflammatory colitis were frequently observed in this cohort.
Abstract
Chronic granulomatous disease (CGD) is a primary immunodeficiency due to alterations in the oxidative metabolism of phagocytic cells. This condition is characterized by serious and recurrent infections caused by pyogenic bacteria, particularly Staphylococcus aureus, and fungal pathogens such as Aspergillus. These infections are associated with granuloma formation and inflammatory manifestations.The aim of our study was to report the clinical characteristics, microbiological aspects and outcomes, and prognosis of a cohort comprising 42 Moroccan patients suffering from CGD. A total of 42 patients were diagnosed for family history, consanguinity, and both clinical and laboratory findings.The diagnosis was confirmed by assessing neutrophil oxidative burst activity, using either the nitroblue tetrazolium (NBT) test or the dihydrorhodamine (DHR) test. The cohort comprised children from 34…
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Taxonomy
TopicsNeutrophil, Myeloperoxidase and Oxidative Mechanisms
