Hereditary nephritis; Hematuria - nephropathy - deafness; Hemorrhagic familial nephritis; Hereditary deafness and nephropathy
Alport syndrome is an inherited disorder that damages the tiny blood vessels in the kidneys. It also causes hearing loss and eye problems.
Alport syndrome is an inherited form of kidney inflammation (nephritis). It is caused by a defect (mutation) in a gene for a protein in the connective tissue, called collagen.
The disorder is rare. There are three genetic types:
- X-linked Alport syndrome (XLAS) -- This is the most common type. The disease is more severe in males than in females.
- Autosomal recessive Alport syndrome (ARAS) -- Males and females have equally severe disease.
- Autosomal dominant Alport syndrome (ADAS) -- This is the rarest type. Males and females have equally severe disease.
With all types of Alport syndrome, the kidneys are affected. The tiny blood vessels in the glomeruli of the kidneys are damaged. The glomeruli filter blood to make urine and remove waste products from the blood.
At first, there are no symptoms. Over time, as the glomeruli are more and more damaged, kidney function is lost and waste products and fluids build up in the body. The condition can progress to end-stage renal disease (ESRD) at an early age, between adolescence and age 40. At this point, dialysis or a kidney transplant is needed.
Symptoms of kidney problems include:
- Abnormal urine color
- Blood in the urine (which can be worsened by upper respiratory infections or exercise)
- Flank pain
- High blood pressure
- Swelling throughout the body
Over time, Alport syndrome also leads to hearing loss. By the early teens, it is common in males with XLAS, though in females, hearing loss is not as common and happens when they're adults. With ARAS, boys and girls have hearing loss during childhood. With ADAS, it occurs later in life.
Hearing loss usually occurs before kidney failure.
Alport syndrome also leads to eye problems, including:
- Abnormal shape of the lens (anterior lenticonus), which can lead to a slow decline in vision as well as cataracts.
- Corneal erosion in which there is loss of the outer layer of the covering of the eyeball, leading to pain, itching, or redness of the eye, or blurred vision.
- Abnormal coloring of the retina, a condition called dot-and-fleck retinopathy. It doesn't cause vision problems, but can help diagnose Alport syndrome.
- Macular hole in which there is thinning or a break in the macula. The macula is a part of the retina that makes central vision sharper and more detailed. A macular hole causes blurred or distorted central vision.
Exams and Tests
The goals of treatment include monitoring and controlling the disease and treating the symptoms.
Your provider may recommend any of the following:
- A diet that limits salt, fluids, and potassium
- Medicines to control high blood pressure
Kidney disease is managed by:
- Taking medicines to slow kidney damage
- A diet that limits salt, fluids, and protein
Hearing loss can be managed with hearing aids. Eye problems are treated as needed. For example, an abnormal lens due to lenticonus or cataracts can be replaced.
Genetic counseling may be recommended because the disorder is inherited.
More information and support for people with Alport syndrome and their families can be found at:
- Alport Syndrome Foundation --
- National Kidney Foundation --
- National Organization for Rare Disorders --
Women usually have a normal lifespan with no signs of the disease except for blood in the urine. In rare cases, women have high blood pressure, swelling, and nerve deafness as a complication of pregnancy.
In men, deafness, vision problems, and end-stage kidney disease are likely by age 50.
As the kidneys fail, dialysis or a transplant will be needed.
When to Contact a Medical Professional
Contact your provider for an appointment if:
- You have symptoms of Alport syndrome.
- You have a family history of Alport syndrome and you are planning to have children.
- Your urine output decreases or stops or you see blood in your urine (this may be a symptom of chronic kidney disease).
Awareness of risk factors, such as a family history of the disorder, may allow the condition to be detected early.
Gregory MC. Alport syndrome and related disorders. In: Gilbert SJ, Weiner DE, eds. National Kidney Foundation's Primer on Kidney Diseases. 7th ed. Philadelphia, PA: Elsevier; 2018:chap 42.
Radhakrishnan J, Appel GB, D'Agati VD. Secondary glomerular disease. In: Yu ASL, Chertow GM, Luyckx VA, Marsden PA, Skorecki K, Taal MW, eds. Brenner and Rector's The Kidney. 11th ed. Philadelphia, PA: Elsevier; 2020:chap 32.
Rheault MN, Kashtan CE. Alport syndrome and other familial glomerular syndromes. In: Feehally J, Floege J, Tonelli M, Johnson RJ, eds. Comprehensive Clinical Nephrology. 6th ed. Philadelphia, PA: Elsevier; 2019:chap 46.
Last reviewed on: 7/27/2021
Reviewed by: Walead Latif, MD, Nephrologist and Clinical Associate Professor, Rutgers Medical School, Newark, NJ. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.