Chronic granulomatous disease
A rare genetic disorder with a predominantly X-linked recessive pattern of inheritance resulting in impaired phagocytic clearance of bacteria and fungi. It is caused by a defect in the phagocytic NADPH oxidase (phox) complex. The phagocytes can engulf pathogens but are unable to produce the microbicidal precursors needed to destroy them. Clinical signs of severe disease present in childhood with milder forms later in life. They include recurrent infection especially pneumonia, cervical lymphadenopathy and hepatosplenomegaly. The clinical course includes the appearance of granulomata in the skin and gastrointestinal or genitourinary tracts. The clinical prognosis is dependent on effectively treating and preventing infection.
Disease Alternative Name
Super Specialist in Reproductive Endocrinology
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PGIMER, Chandigarh
MD
Self Emploid(private Clinic)
Morbi
Shri M P Shah Medical College Jamnagar
M B B S
Konaseema Inst. of Medical Sciences Research Foundation
Campus Ambassasor for Smarc 2018
Konaseema Inst. of Medical Sciences Research Foundation
MBBS
Shree Krishna Hospital
Resident
Pramukhswami Medical College
MD, INTERNAL MEDICINE
Government Hospital,Siddhartha Medical College
Student
St.Gabriels High School
20 Years of Teaching To Both UGs & PGs
As Assistant, Associate & Professor
Gandhi Medical College, Dr. NTRUHS
MD Pathology
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