(See also Overview of Nephritic Syndrome Overview of Nephritic Syndrome Nephritic syndrome is defined by hematuria, variable degrees of proteinuria, usually dysmorphic red blood cells (RBCs), and often RBC casts on microscopic examination of urinary sediment. Often... read more .)
Alport syndrome is a nephritic syndrome caused by a mutation in the COL4A3, COL4A4, and COL4A5 genes that encode the alpha-5 chain of type IV collagen and results in altered type IV collagen strands. The mechanism by which collagen alteration causes a glomerular disorder is unknown, but impaired structure and function are presumed; in most families, thickening and thinning of the glomerular and tubular basement membranes occur, with multilamination of the lamina densa in a focal or local distribution (basket-weave pattern). Glomerular scarring and interstitial fibrosis eventually result.
The disorder is most commonly inherited in X-linked fashion, although autosomal recessive and, rarely, autosomal dominant varieties exist. Cases with X-linked inheritance may be clinically categorized as
Classic X-linked disease in males and autosomal recessive disease are clinically similar. Patients develop renal symptoms and signs similar to those of acute nephritic syndrome (eg, microscopic hematuria, hypertension, eventually gross hematuria with proteinuria) and progress to renal insufficiency between ages 20 and 30 (juvenile forms).
Sensorineural hearing loss frequently is present, affecting higher frequencies; it may not be noticed during early childhood.
Ophthalmologic abnormalities—cataracts (most common), anterior lenticonus (a regular conical protrusion on the anterior aspect of the lens due to thinning of the lens capsule), spherophakia (spherical lens deformation that can predispose to lens subluxation), nystagmus, retinitis pigmentosa, blindness—also occur but less frequently than hearing loss.
X-linked disease occurs in heterozygous women, who, because they have one normal X chromosome, usually have less severe, more slowly progressing symptoms than men.
Some men with X-linked disease develop renal insufficiency after age 30 with hearing loss that occurs late or is mild, and autosomal dominant disease typically does not cause renal failure until age ≥ 45 years (adult forms).
In patients with X-linked Alport syndrome, sensorineural hearing loss usually manifests in childhood, whereas renal disease often does not manifest until adulthood.
Other nonrenal manifestations rarely include polyneuropathy Polyneuropathy A polyneuropathy is a diffuse peripheral nerve disorder that is not confined to the distribution of a single nerve or a single limb and typically is relatively symmetrical bilaterally. Electrodiagnostic... read more and thrombocytopenia Thrombocytopenia: Other Causes Platelet destruction can develop because of immunologic causes (viral infection, drugs, connective tissue or lymphoproliferative disorders, blood transfusions) or nonimmunologic causes (sepsis... read more .
Diagnosis is suggested in patients who have microscopic hematuria on urinalysis or recurrent episodes of gross hematuria, particularly if an abnormality of hearing or vision or a family history of chronic kidney disease Chronic Kidney Disease Chronic kidney disease (CKD) is long-standing, progressive deterioration of renal function. Symptoms develop slowly and in advanced stages include anorexia, nausea, vomiting, stomatitis, dysgeusia... read more is present.
Urinalysis and usually renal biopsy Renal biopsy Biopsy of the urinary tract requires a trained specialist (nephrologist, urologist, or interventional radiologist). Indications for diagnostic biopsy include unexplained nephritic or nephrotic... read more are done. In addition to dysmorphic red blood cells, the urine may contain protein, white blood cells, and casts of various types. Nephrotic syndrome occurs rarely. No distinguishing histologic changes are seen on light microscopy. The diagnosis can be confirmed by any of the following:
Renal biopsy with immunostaining for the subtypes of type IV collagen
Characteristic disorganization of the lamina densa with variable thickening and thinning of the glomerular capillary basement membrane seen using electron microscopy
Skin biopsy with immunostaining for the type IV collagen subtypes in a patient with a positive family history
Molecular genetic analysis of the COL4A genes
A combination of immunostaining and electron microscopy is often needed to distinguish Alport syndrome from some forms of thin basement membrane disease Thin Basement Membrane Disease Thin basement membrane disease is diffuse thinning of the glomerular basement membrane from a width of 300 to 400 nm in normal subjects to 150 to 225 nm. (See also Overview of Nephritic Syndrome... read more .
Treatment is indicated only when uremia occurs; its management is the same as that for other causes of chronic kidney disease Treatment Chronic kidney disease (CKD) is long-standing, progressive deterioration of renal function. Symptoms develop slowly and in advanced stages include anorexia, nausea, vomiting, stomatitis, dysgeusia... read more . Anecdotal reports suggest that angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers may slow progression of renal disease. Transplantation Kidney Transplantation Kidney transplantation is the most common type of solid organ transplantation. (See also Overview of Transplantation.) The primary indication for kidney transplantation is End-stage renal failure... read more has been successful, but antiglomerular basement membrane antibody disease may occur, usually only in males, in the transplanted kidney. Genetic counseling is indicated.
Consider Alport syndrome if patients have hematuria plus a hearing and/or vision abnormality or a family history of chronic kidney disease.
Confirm the diagnosis by biopsy of the kidney or sometimes skin and immunostaining for type IV collagen subtypes or molecular genetic testing.
Treat chronic kidney disease and consider transplantation.