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         Alport Syndrome:     more detail
  1. Molecular Pathology and Genetics of Alport Syndrome (Contributions to Nephrology)
  2. Alport Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19
  3. Gale Encyclopedia of Medicine: Alport syndrome by Carol A. Turkington, 2002-01-01
  4. The Molecular Genetics of X-Linked Alport Syndrome (Acta Biomedica Lovaniensia) by Caiying Guo, 1995-11
  5. Alport Syndrome: An entry from Gale's <i>Gale Encyclopedia of Medicine, 3rd ed.</i> by Carol Turkington, 2006
  6. Hereditary nephropathy with hearing loss: "Alport's syndrome" (Acta paediatrica Scandinavica : Supplement) by Ulla Marianne Iversen, 1974
  7. Hereditary hearing loss with nephropathy (Alport's syndrome); (Acta oto-laryngologica. Supplement[um]) by John Sidney Turner, 1970
  8. Familial nephritis: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Maria, PhD Basile, 2005

21. Alport Syndrome And Mental Retardation Clinical And Genetic
Your browser does not support frames. Click here to view the unframed reprint.
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22. National Kidney Foundation: A To Z Health Guide
Welcome to the National Kidney Foundation s Kidney Learning System.
http://www.kidney.org/atoz/atozItem.cfm?id=47

23. Alport Syndrome And Mental Retardation Clinical And Genetic
alport syndrome and mental retardation clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATSMR)
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

24. GeneReviews: Alport Syndrome
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http://www.geneclinics.org/profiles/alport
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25. Alport Syndrome
alport syndrome. Pediatric Database Home Page. alport syndrome Home Page. http//www.cc.utah.edu/~cla6202/ASHP.htm . The Hereditary Nephritis Foundation
http://www.healthatoz.com/healthatoz/Atoz/ency/alport_syndrome.jsp

26. Alport Syndrome - Genetics Home Reference
alport syndrome is a genetic condition characterized by the progressive loss of alport syndrome can also affect the eyes. The presence of blood in the
http://ghr.nlm.nih.gov/condition=alportsyndrome
Home What's New Browse Handbook ... Search Alport syndrome
Alport syndrome
On this page:
What is Alport syndrome?
Alport syndrome is a 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. Many people with Alport syndrome also exhibit high levels of protein in their urine (proteinuria). As this condition progresses, the kidneys become less able to function properly and kidney failure results. Hearing loss is a common feature of Alport syndrome, but the abnormalities in the eyes seldom lead to loss of vision.
How common is Alport syndrome?

27. Alport Syndrome - References - Genetics Home Reference
Xlinked alport syndrome natural history and genotype-phenotype Familial hematuria due to type IV collagen mutations alport syndrome and thin basement
http://ghr.nlm.nih.gov/condition=alportsyndrome/show/References
Home What's New Browse Handbook ... Search Alport syndrome
Alport syndrome
References
These sources were used to develop the Genetics Home Reference condition summary on Alport syndrome. Last Comprehensive Review: January 2005 Published: September 6, 2005

28. Alport Syndrome
alport syndrome is an inherited disorder (usually Xlinked) involving damage to the kidney, , and in some families, loss of hearing.
http://www.healthcentral.com/ency/408/000504.html
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Definition: Alport syndrome is an inherited disorder (usually X-linked) involving damage to the kidney

29. Page Not Found - Boys Town National Research Hospital
alport syndrome (AS) is characterized by hereditary nephritis (kidney disease known as Bright s disease in the past) and sensorineural hearing loss.
http://www.boystownhospital.org/parents/info/genetics/alport.asp
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30. Alport Syndrome Definition - Medical Dictionary Definitions Of Popular Medical T
Online Medical Dictionary and glossary with medical definitions.
http://www.medterms.com/script/main/art.asp?articlekey=10745

31. Urologic And Male Genital Diseases
alport syndrome and Hearing Boystown Hospital. in FOCUS JF Martin. About Alport s Syndrome - Kidney Foundation of Canada
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Diseases and Disorders Links pertaining to Urologic and Male Genital Diseases Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Anti-Glomerular Basement Membrane Disease Balanitis Bladder Diseases Bladder Exstrophy ... Vesico-Ureteral Reflux
Urologic and Male Genital Diseases Nephrology and Urology - The Family Practice Handbook, University of Iowa (US) Catheterization Basics - NursingCEU.com About the Foley Catheter - eMedicine/Consumer Health
Fournier Gangrene About Fournier Gangrene [Santora and Rukstalis] - eMedicine
Genital Diseases, Male Male Genital System Pathology [images; EC Klatt] Sex Organ Homologies - Loyola Univ. (US) Sexually Transmitted Diseases, Bacterial [links] Ed's Lecture Notes on Diseases of the Male Reproductive System [E Friedlander] - (US) [GT Falk] - (UK) The Circumcision Debate - Dr. George

32. Alport Syndrome
Phenotypic and genotypic features of alport syndrome in Chinese children. Chinese alport syndrome (AS) was analyzed in 44 unrelated patients who were
http://www.thedoctorsdoctor.com/diseases/alport_syndrome.htm
Background This is a rare inherited disease that chiefly affects the kidneys. It is caused by mutations in one or the other of several COL4A genes. These genes encode for the elements of the basement membrane (Type IV) collagen. The result is a hereditary glomerulonephritis with a chronic nephritis that progresses to end-stage renal disease. Associated conditions include hearing loss, lenticonus and other eye disorders, immunologic abnormality of skin, disorders of platelets, abnormalities of white blood cells, and smooth muscle tumors. OUTLINE Epidemiology Disease Associations Pathogenesis Laboratory/Radiologic/Other Diagnostic Testing ... Internet Links EPIDEMIOLOGY CHARACTERIZATION SYNONYMS X-linked hereditary nephritis INCIDENCE/PREVALENCE About 5000 individuals worldwide AGE SEX GEOGRAPHY CHINESE
Phenotypic and genotypic features of Alport syndrome in Chinese children. Wang F, Ding J, Guo S, Yang J. Department of Pediatrics, First Hospital, Peking University, Beijing, China.
Pediatr Nephrol 2002 Dec;17(12):1013-20 Abstract quote

33. NORD - National Organization For Rare Disorders, Inc.
alport syndrome is a group of hereditary disorders characterized by progressive Some types of alport syndrome may also affect vision and hearing.
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Alport Syndro

34. CCHS Clinical Digital Library
alport syndrome English Spanish. Miscellaneous alport syndrome Patients/Family Resources. Healthfinder (US DHHS) Homepage
http://cchs-dl.slis.ua.edu/patientinfo/nephrology/glomerulonephritis/multi/alpor
Patient/Family Resources by Topic: Nephrology
Alport Syndrome Patient/Family Resources
Spanish Miscellaneous See also:

35. CCHS Clinical Digital Library
Hereditary Nephritis, Including alport syndrome Access document Hereditary Nephritis (Alport s Syndrome), Microscopic Access document
http://cchs-dl.slis.ua.edu/clinical/nephrology/glomerulonephritis/multisystem/al
Clinical Resources by Topic: Nephrology
Alport Syndrome Clinical Resources
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36. AllRefer Health - Alport Syndrome (Hematuria - Nephropathy - Deafness, Hemorrhag
alport syndrome (Hematuria Nephropathy - Deafness, Hemorrhagic Familial Nephritis, Hereditary Deafness and Nephropathy, Hereditary Nephritis) information
http://health.allrefer.com/health/alport-syndrome-info.html

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Alternate Names : Hematuria - Nephropathy - Deafness, Hemorrhagic Familial Nephritis, Hereditary Deafness and Nephropathy, Hereditary Nephritis Definition Alport syndrome is an inherited (usually X-linked) disorder involving damage to the kidney, blood in the urine , and in some families, loss of hearing . The disorder may also include eye defects
Male Urinary System Alport syndrome is very similar to hereditary nephritis. There may be nerve deafness and congenital eye abnormalities associated with Alport syndrome. The cause is a mutation in a gene for collagen. The disorder is uncommon, and most often affects males since the genetic defect is typically found on the X chromosome.

37. AllRefer Health - Alport Syndrome Treatment (Hematuria - Nephropathy - Deafness,
alport syndrome (Hematuria Nephropathy - Deafness, Hemorrhagic Familial Nephritis, Hereditary Deafness and Nephropathy, Hereditary Nephritis) information
http://health.allrefer.com/health/alport-syndrome-treatment.html

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Alternate Names : Hematuria - Nephropathy - Deafness, Hemorrhagic Familial Nephritis, Hereditary Deafness and Nephropathy, Hereditary Nephritis Alport Syndrome Treatment Treatment goals include monitoring and controlling progression of the disease and treatment of symptoms. The most important task is strict control of high blood pressure
Treatment of chronic renal failure will become necessary. This may include dietary modifications, fluid restriction, and other treatments. Ultimately, chronic renal failure progresses to

38. Alport Syndrome Medical Information
alport syndrome Information from Drugs.com. alport syndrome is very similar to hereditary nephritis. There may be nerve deafness and congenital eye
http://www.drugs.com/enc/alport_syndrome.html

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Alport syndrome
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Alport syndrome
Definition
Alport syndrome is an inherited disorder (usually X-linked) involving damage to the kidney, blood in the urine , and in some families, loss of hearing. The disorder may also include eye defects.
Alternative Names
Hereditary nephritis; Hematuria - nephropathy - deafness; Hemorrhagic familial nephritis; Hereditary deafness and nephropathy
Causes
Alport syndrome is very similar to hereditary nephritis. There may be nerve deafness and congenital eye abnormalities associated with Alport syndrome. The cause is a mutation in a gene for collagen. The disorder is uncommon, and most often affects males since the genetic defect is typically found on the X chromosome. In women, the disorder is usually mild, with minimal or no symptoms. Women can transmit the gene for the disorder to their children, even if the woman has no symptoms of the disorder. In men, the symptoms are more severe and progress faster.

39. ► Alport Syndrome
A medical encycopedia article on the topic alport syndrome.
http://www.umm.edu/ency/article/000504.htm
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Alport syndrome
Overview Symptoms Treatment Prevention Definition: Alport syndrome is an inherited (usually X-linked) disorder involving damage to the kidney, blood in the urine , and in some families, loss of hearing . The disorder may also include eye defects
Alternative Names: Hereditary nephritis; Hematuria - nephropathy - deafness; Hemorrhagic familial nephritis; Hereditary deafness and nephropathy
Causes, incidence, and risk factors: Alport syndrome is very similar to hereditary nephritis. There may be nerve deafness and congenital eye abnormalities associated with Alport syndrome. The cause is a mutation in a gene for collagen. The disorder is uncommon, and most often affects males since the genetic defect is typically found on the X chromosome.
In women, the disorder is usually mild, with minimal or no symptoms. Women can transmit the gene for the disorder to their children, even if the woman has no symptoms of the disorder. In men, the symptoms are more severe and progress faster.
The disorder causes chronic glomerulonephritis with destruction of the glomeruli. Initially, there are no symptoms. Progressive destruction of the glomeruli causes

40. BBC - Health - Conditions - Alport Syndrome
A guide to alport syndrome which causes kidney failure.
http://www.bbc.co.uk/health/conditions/alport1.shtml
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Alport syndrome
Dr Trisha Macnair Dr Trisha Macnair Those affected by alport syndrome develop progressive loss of renal (kidney) function, and sometimes progressive deafness and abnormalities of the eye.
In this article
What is it? Who's affected? Diagnosis Treatment
What is it?
Alport syndrome is the second most common inheirited cause of kidney failure. There are many other, much more common, acquired causes of kidney failure, such as diabetes, high blood pressure and glomerulonephritis (inflammation of the kidney that may develop for a variety of reasons). It occurs when a special type of collagen normally found in the kidney is missing or abnormal. One of the early signs of alport syndrome may be small amounts of blood or protein in the urine during childhood.
Who's affected?
It's more common among males About one in 5,000 children are affected by alport syndrome. Because of the way in which it's inherited, it's more common among males. The gene that causes most cases (called COL4A5) is on the X chromosome. Women have two X chromosomes, so they usually have a healthy gene as well as the faulty one, but men don't because they have an X chromosome and a Y one. Women who carry the faulty gene may have minor kidney problems and sometimes more serious kidney disease.

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