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| | '''For patient information on this page, click [[Alport syndrome (patient information)|here]]''' |
| {{DiseaseDisorder infobox | | | {{DiseaseDisorder infobox | |
| Name = Alport syndrome | | | Name = Alport syndrome | |
| ICD10 = {{ICD10|Q|87|8|q|80}} | | | ICD10 = {{ICD10|Q|87|8|q|80}} | |
| ICD9 = {{ICD9|759.89}} | | | ICD9 = | |
| ICDO = | | | ICDO = | |
| Image = | | | Image = | |
| Caption = | | | Caption = | |
| OMIM = 301050 | | | OMIM = 301050 | |
| OMIM_mult = {{OMIM2|104200}} {{OMIM2|203780}} {{OMIM2|300195}} | | | OMIM_mult = {{OMIM2|104200}} {{OMIM2|203780}}| |
| MedlinePlus = 000504 | | | MedlinePlus = 000504 | |
| eMedicineSubj = |
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| eMedicineTopic = |
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| DiseasesDB = 454 | | | DiseasesDB = 454 | |
| MeshID = D009394 | | | MeshID = D009394 | |
| }} | | }} |
| {{Search infobox}} | | {{Alport syndrome}} |
| '''For patient information on this page, click [[Alport syndrome (patient information)|here]]'''
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| {{CMG}}; {{AE}} {{AN}} | | {{CMG}}; {{AE}} {{AN}} |
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| '''''Synonyms and keywords:''''' Hereditary nephritis, hemorrhagic familial nephritis
| | {{SK}} Hereditary nephritis; hemorrhagic familial nephritis; X-linked nephropathy and deafness; hematuria-nephropathy-deafness; hereditary deafness and nephropathy |
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| ==Overview==
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| '''Alport syndrome''' is a [[genetic disorder|genetic]] condition characterized by the progressive loss of [[kidney]] function and hearing. Alport syndrome can also affect the eyes. The presence of [[blood]] in the [[urine]] ([[hematuria]]) is almost always found in this condition.
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| ==Historical Perspective==
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| Alport syndrome was first identified in a British family by Dr. [[Cecil A. Alport]] in 1927.
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| ==Pathophysiology==
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| ===Genetics===
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| Alport syndrome is caused by [[mutation]]s in the ''[[COL4A3]]'', ''[[COL4A4]]'', and ''[[COL4A5]]'' [[collagen]] biosynthesis genes. Mutations in any of these genes prevent the proper production or assembly of the [[type IV collagen]] network, which is an important structural component of the [[glomerular basement membrane]]s in the [[kidney]], inner [[ear]], and [[eye]].
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| This syndrome can have different inheritance patterns depending on the type of genetic mutation. In most people with Alport syndrome, the condition is inherited in an [[X-linked]] pattern, due to mutations in the ''COL4A5'' gene. A condition is considered X-linked if the gene involved in the disorder is located on the [[X chromosome]].
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| Alport syndrome can also be inherited in an [[autosomal recessive]] pattern if both copies of the ''COL4A3'' or ''COL4A4'' gene, located on [[chromosome 2 (human)|chromosome 2]], have been mutated. Most often, the parents of a child with an autosomal recessive disorder are not affected but are only carriers of one copy of the altered genes.
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| In males, who have only one X chromosome, one altered copy of the ''COL4A5'' gene is sufficient to cause severe Alport syndrome, which explains why most affected males eventually develop [[chronic kidney failure]]. In females, who have two X chromosomes, a mutation in one copy of the ''COL4A5'' gene usually results in blood in the urine, but most affected females do not develop kidney failure.
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| ===Associated Conditions===
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| Some associated conditions that occur with Alport syndrome are [[chronic kidney failure]], and [[proteinuria]].
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| ===Microscopic Pathology===
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| Basement membranes are thin, sheet-like structures that separate and support cells in many tissues. When mutations prevent the formation of type IV collagen fibers, the basement membranes of the [[kidneys]] are not able to filter waste products from the blood and create urine normally, allowing blood and [[protein]] to enter into the urine.
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| The abnormalities of type IV collagen in the [[glomerular basement membrane]] cause gradual scarring of the [[kidneys]], eventually leading to [[chronic renal failure]] in many people with the disease.
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| —==Diagnosis==
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| ===Diagnostic criteria===
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| Gregory et al, 1996, give the following 10 criteria for the diagnosis of Alport syndrome <ref name="pmid8801040">{{cite journal |author=Gregory MC, Terreros DA, Barker DF, Fain PN, Denison JC, Atkin CL |title=Alport syndrome--clinical phenotypes, incidence, and pathology |journal=Contrib Nephrol |volume=117 |issue= |pages=1–28 |year=1996 |pmid=8801040 |doi= |url=}}</ref>. 4 of the 10 criteria must be met for an accurate diagnosis:
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| * Family history of [[nephritis]] and of unexplained [[hematuria]] in a first degree relative of the [[index case]] or in a male relative linked through any numbers of females.
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| * Persistent [[hematuria]] without evidence of another possibly inherited nephropathy such as [[thin GBM disease]], [[polycystic kidney disease]] or [[IgA nephropathy]].
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| * Bilateral [[sensorineural hearing loss]] in the 2000 to 8000 Hz range. The hearing loss develops gradually, is not present in early infancy and commonly presents before the age of 30.
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| * A [[mutation]] in a COL4An gene (where n = 3, 4 or 5).
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| * [[Immunohistochemistry|Immunohistochemical]] evidence of complete or partial lack of the Alport [[epitope]] in glomerular, or epidermal basement membranes, or both.
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| * Widespread [[GBM|glomerular basement membrane]] ultrastructural abnormalities, in particular thickening, thinning and splitting.
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| * Ocular lesions including anterior lenticonus, posterior subcapsular [[cataract]], posterior polymorphous dystrophy and [[retinal flecks]].
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| * Gradual progression to [[ESRD]] in the index case of at least two family members.
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| * [[Macrothrombocytopenia]] or [[granulocytic inclusions]].
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| * Diffuse [[leiomyomatosis]] of the [[esophagus]] or [[female genitalia]], or both.
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| ===Symptoms===
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| Common symptoms of Alport syndrome include:
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| *[[Hematuria]]
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| *[[Peripheral edema]], [[anasarca]]
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| *Decrease or [[loss of vision]]
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| *Difficulty hearing
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| *Flank pain
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| *[[Eye pain]]
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| *[[Lacrimation]]
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| *[[Photophobia]]
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| ===Physical Examination===
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| ====Vital signs====
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| *[[Systemic hypertension]]
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| ====Eyes====
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| [[Fundoscopy]] shows:
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| *[[Cataract]]s
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| *Subcapsular posterior lens opacities
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| *[[Lenticonus]]
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| *Retinal flecks (dot-and-fleck retinopathy)
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| *Posterior polymorphous corneal dystrophy/corneal epithelial erosions
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| ====Ears====
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| *[[Sensorineural deafness]]
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| ====Extremities====
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| *[[Peripheral edema]]
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| *[[Anasarca]]
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| *[[Leimyomatosis]]
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| ===Laboratory Findings===
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| ====Urinalysis====
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| *Microscopic [[hematuria]]
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| *[[Pyuria]]
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| *Red cell [[casts]]
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| *Cylindrical [[casts]]
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| *[[Proteinuria]]
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| ====Electrolytes and Metabolic disturbances====
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| *Increased [[BUN]]
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| *Increased [[serum creatinine]] levels
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| *[[Hypoalbuminemia]]
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| ====Renal biopsy==== | | ==[[Alport syndrome overview|Overview]]== |
| *Irregularly thin and attenuated [[glomerular basement membrane]]
| | ==[[Alport syndrome historical perspective|Historical Perspective]]== |
| *Splitting of [[glomerular basement membrane]]
| | ==[[Alport syndrome pathophysiology |Pathophysiology]]== |
| *Scarring of tubules and interstitium
| | ==[[Alport syndrome causes|Causes]]== |
| | ==[[Alport syndrome differential diagnosis|Differentiating Alport syndrome from other Diseases]]== |
| | ==[[Alport syndrome epidemiology and demographics|Epidemiology and Demographics]]== |
| | ==[[Alport syndrome natural history, complications and prognosis|Natural History, Complications and Prognosis]]== |
| | ==Diagnosis== |
| | [[Alport syndrome diagnostic criteria|Diagnostic Criteria]] | [[Alport syndrome history and symptoms|History and Symptoms]] | [[Alport syndrome physical examination|Physical Examination]] | [[Alport syndrome laboratory findings|Laboratory Findings]] | [[Alport syndrome echocardiography or ultrasound|Echocardiography or Ultrasound]] | [[Alport syndrome other diagnostic studies|Other Diagnostic Studies]] |
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| ==Treatment== | | ==Treatment== |
| *As there is no known cure for the condition, treatments are symptomatic.
| | [[Alport syndrome medical therapy|Medical Therapy]] | [[Alport syndrome surgery|Surgery]] | [[Alport syndrome primary prevention|Primary Prevention]] | [[Alport syndrome secondary prevention|Secondary Prevention]] | [[Alport syndrome cost-effectiveness of therapy|Cost-Effectiveness of Therapy]] | [[Alport syndrome future or investigational therapies|Future or Investigational Therapies]] |
| *Patients are advised on how to manage the complications of [[chronic kidney failure]] and the [[proteinuria]] that develops is often treated with [[ACE inhibitors]], although they are not always used simply for the [[hypertension]].
| | ==Case Studies== |
| *Once kidney failure has developed, patients are given [[dialysis]] or can benefit from a [[kidney transplant]], although this can cause problems.
| | :[[Alport syndrome case study one|Case #1]] |
| *The body may reject the new kidney as it contains normal type IV collagen, which may be recognized as foreign by the immune system.
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| *[[Gene therapy]] as a possible treatment option has been discussed.<ref name="pmid9150464">{{cite journal |author=Tryggvason K, Heikkilä P, Pettersson E, Tibell A, Thorner P |title=Can Alport syndrome be treated by gene therapy? |journal=Kidney Int. |volume=51 |issue=5 |pages=1493–9 |year=1997 |month=May |pmid=9150464 |doi= |url=}}</ref>
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| ==References== | |
| {{reflist|2}}
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| ''This article incorporates public domain text from [http://ghr.nlm.nih.gov The U.S. National Library of Medicine]'' | | ''This article incorporates public domain text from [http://ghr.nlm.nih.gov The U.S. National Library of Medicine]'' |
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| ==External links==
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| [http://www.moldiag.de/en/dis/alport.htm Laboratory for Molecular Diagnostics, Center for Nephrology and Metabolic Disorders, Dr Mato Nagel]
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| {{Phakomatoses and other congenital malformations not elsewhere classified}}
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| [[Category:Genetic disorders]] | | [[Category:Genetic disorders]] |
| [[Category:Kidney diseases]] | | [[Category:Kidney diseases]] |
| [[Category:Syndromes]] | | [[Category:Syndromes]] |
| [[Category:Disease]] | | [[Category:Disease]] |
| [[Category:Grammar]]
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