Alport Syndrome Pathophysiology

Loading...

Alport syndrome is a genetic disorder [1] affecting around 1 in 50,000 children, characterized by glomerulonephritis , end-stage kidney disease, and hearing loss. [2] Alport syndrome can also affect the eyes, though the changes do not usually affect sight, except when changes to the lens occur in later life. Blood in urine is universal. Proteinuria is a feature as kidney disease progresses.

Presentation on nephrotic syndrome

or Hereditary Nephritis

Medical Addicts: Eisenmenger syndrome Pathophysiology

Causes of Glomerulonephritis

NEPHROTIC SYNDROME by EKE E.P.

Renal - Physiology 210 with Saswati at University of ...

PATHOPHYSIOLOGY OF VASCULAR TONE

Heal Yourself At Home

Cystic Fibrosis Symptoms

Bowman's capsule - Wikipedia

soutenons les drepanocytaires

Prader-Willis syndrom

Nephropathy: Nephropathy Wiki