Infantile malignant osteopetrosis (IMO) is a rare genetic disorder characterized by excessively dense bones due to defective bone resorption. This condition, also known as malignant…
Infantile hypophosphatasia (HPP) is a rare genetic disorder that affects bone mineralization, leading to skeletal deformities, respiratory issues, and severe developmental concerns. This condition occurs…
Infant botulism is a rare but serious illness caused by the ingestion of Clostridium botulinum spores, which produce a powerful neurotoxin in the baby's intestines.…
Atherosclerotic cardiovascular disease (ASCVD) is a progressive condition characterized by the accumulation of plaque in the arteries, leading to narrowed or blocked vessels. This condition…
Inclusion conjunctivitis is an ocular infection primarily caused by the bacterium Chlamydia trachomatis. This condition is commonly transmitted through genital-ocular contact but can also result…
Inclusion body myositis (IBM) is a rare, progressive muscle disorder characterized by inflammation, muscle weakness, and degeneration. IBM primarily affects older adults, typically over the…
Inactive tuberculosis, also known as latent TB infection (LTBI), occurs when an individual is infected with Mycobacterium tuberculosis bacteria but does not exhibit active symptoms.…
Impetigo is a common and highly contagious bacterial skin infection that predominantly affects infants and young children. It manifests as red sores that rupture, ooze…
Immunoglobulin deficiency refers to a medical condition in which the body's immune system lacks adequate immunoglobulins (antibodies) to fight infections effectively. These antibodies are critical…
Immunoglobulin A nephropathy (IgAN), also known as Berger's disease, is a kidney disorder characterized by the accumulation of Immunoglobulin A (IgA) deposits in the glomeruli.…