Inheritance pattern and clinical aspects of 93 Iranian patients with chronic granulomatous disease

F Fattahi, M Badalzadeh, L Sedighipour… - Journal of clinical …, 2011 - Springer
F Fattahi, M Badalzadeh, L Sedighipour, M Movahedi, MR Fazlollahi, SD Mansouri…
Journal of clinical immunology, 2011Springer
Background Chronic granulomatous disease (CGD) is a rare immunodeficiency due to a
genetic defect in one of the NADPH-oxidase components. We studied CGD inheritance
forms (autosomal recessive (AR) or X-linked (XL)) and AR-CGD subtypes in Iran. Methods
Clinical and functional investigations were conducted in 93 Iranian CGD patients from 75
families. Results Most of the patients were AR-CGD (87.1%). This was related to
consanguineous marriages (p= 0.001). The age of onset of symptoms and diagnosis were …
Background
Chronic granulomatous disease (CGD) is a rare immunodeficiency due to a genetic defect in one of the NADPH-oxidase components. We studied CGD inheritance forms (autosomal recessive (AR) or X-linked (XL)) and AR-CGD subtypes in Iran.
Methods
Clinical and functional investigations were conducted in 93 Iranian CGD patients from 75 families.
Results
Most of the patients were AR-CGD (87.1%). This was related to consanguineous marriages (p = 0.001). The age of onset of symptoms and diagnosis were lower in XL-CGD compared with AR-CGD (p < 0.0001 for both). Among AR-CGD patients, p47phox defect was the predominant subtype (55.5%). The most common clinical features in patients were lymphadenopathy (65.6%) and pulmonary involvement (57%). XL-CGD patients were affected more frequently with severe infectious manifestations.
Conclusions
Although XL-CGD is the most common type of the disease worldwide, only 12 patients (12.9%) were XL-CGD in our study. The relatively high frequency of AR-CGD is probable due to widely common consanguineous marriages in Iran.
Springer
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