phagocytic disorder

phagocytic disorder

Phagocytic disease Immunology Any rare qualitative disorder of phagocytic WBCs, which may be familial and accompanied by generalized metabolic dysfunction; the  prototypic PD is chronic granulomatous disease. See Chronic granulomatous disease. Cf Histiocytic diseases.
Phagocytic Disorders
Structural & functional defects
Alder-Reilly anomaly
•  Chédiak-Higashi anomaly
•  Familial vacuolization of leukocytes (Jordan's anomaly)
•  May-Hegglin anomaly
•  Pelger-Huët anomaly
•  Pseudo- (or acquired) Pelger-Huët anomaly
•  Hereditary giant neutrophilia
•  Hereditary hypersegmentation of neutrophilic nuclei
Functional defects–without structural changes
•  Chronic granulomatous disease
•  Myeloperoxidase deficiency
•  CD11/CD18 adhesive protein deficiency
•  Other enzyme defects  
References in periodicals archive ?
The first specimen from a patient having chronic granulomatous disease, a phagocytic disorder, tested positive for echovirus 14, but the patient died before the next specimen collection (Table 3).
Less common primary immunodeficiencies affect 1 in 50,000 to 1 in 200,000 children and include B-cell disorders, T-cell disorders, phagocytic disorders, and complement disorders, he said at the meeting.
section]) Includes B-(humoral) or T-lymphocyte deficiency, complement deficiencies (particularly Cl, C2, C3, and C4 deficiencies), and phagocytic disorders (excluding chronic granulomatous disease).
section]) Including B-(humoral) or T-lymphocyte deficiency, complement deficiencies (particularly C1, C2, C3, and C4 deficiencies), and phagocytic disorders (excluding chronic granulomatous disease).