Retinitis pigmentosa is a genetically determined degeneration of the retina, in which the photoreceptors of the eyes perish bit by bit and thus in the late course of the disease usually complete blindness occurs. Frequently, this phenomenon is only one symptom of several and, together with the respective accompanying symptoms, forms an entire symptom complex, … Retinitis Pigmentosa: Causes, Symptoms & Treatment
IgA nephritis is the most common disease of the renal corpuscles. It is classified as idiopathic glomerulonephritis. What is IgA nephritis? IgA nephritis is a kidney disease that is associated with hematuria and gradually leads to limitations in kidney function. Deposits of immunoglobulin A (IgA) on the kidney corpuscles (glomeruli) are responsible. IgA nephritis is … IgA Nephritis: Causes, Symptoms & Treatment
Ectrodactyly is a skeletal deformity of the hands or feet. The condition is often genetic and exists from birth in affected individuals. In the context of ectrodactyly, the affected patients show mutilations of the fingers or feet. In numerous cases, fingers or individual toes are missing. This often results in the appearance of a so-called … Ectrodactyly: Causes, Symptoms & Treatment
Alport syndrome is a hereditary disease. It primarily affects the kidneys, eyes, and inner ear. What is Alport syndrome? Doctors also refer to Alport syndrome as progressive hereditary nephritis. This refers to a hereditary disease that causes progressive nephropathy leading to kidney failure. Physicians also refer to Alport syndrome as progressive hereditary nephritis. This refers … Alport Syndrome: Causes, Symptoms & Treatment
