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  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

81. MediFocus MedCenter Preview For Alport's Syndrome
MediFocus MedCenter © 33 alport's syndrome (NK001) Introduction Nephritis issuesWhat are the most common symptoms of alport's syndrome?
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Alport's Syndrome
Introduction
Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
AS affects the basement membranes which are the supporting layers of epithelial and endothelial tissues that make up much of the body's surfaces. The cause is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people.
Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
The cause of AS is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people. Treatment requires medication, and often, kidney transplant.

82. MediFocus MedCenter Preview For Alport's Syndrome
MediFocus MedCenter © alport's syndrome (NK001) Introduction. Nephritis issuesWhat are the most common symptoms of alport's syndrome?
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Alport's Syndrome
Introduction
Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
AS affects the basement membranes which are the supporting layers of epithelial and endothelial tissues that make up much of the body's surfaces. The cause is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people.
Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
The cause of AS is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people. Treatment requires medication, and often, kidney transplant.

83. BBC Health - Ask The Doctor - Alport's Syndrome
Ask the Doctor. Q alport's syndrome. I am trying to find out some informationabout alport's syndrome, can you help? What is it, is it curable? Gillian.
http://www.bbc.co.uk/health/ask_doctor/alports_syndrome.shtml

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Q: Alport's Syndrome I am trying to find out some information about Alport's Syndrome, can you help? What is it, is it curable? Gillian Dr Trisha Macnair responds Alport's Syndrome is a rare inherited problem which has a combination of the effects. Most commonly the kidneys are affected, with nephritis (inflammation) and the gradual development of kidney failure. But hearing may also be affected (there is nerve deafness - i.e. it is the nerves which detect hearing which are to blame rather than structures in the ear or brain). Very rarely there may also be problems with the platelets in the blood, which are tiny cells that normally control the 'stickiness' and clotting of blood. It's much more common in boys Because it is inherited , several people in one family may have the same problem. Alport's is unusual because it is one of the few problems thought to be carried on the X chromosome (the 'female" chromosome). Girls are protected to a degree because they carry two X chromosomes and so may have a normal copy of the gene as well as the faulty one. However, boys carry one X and one Y chromosome, and so those who carry a faulty gene have no normal X to protect them. This is why men develop Alport's Syndrome more often than women. But there are several different types of Alport's Syndrome and the exact way in which it is inherited is still under debate.

84. Alport's Syndrome
alport's syndrome, This fact sheet focuses on alport's syndrome (a genetic diseasethat causes progressive kidney damage), published in April 2001.
http://omni.ac.uk/whatsnew/detail/4052205.html

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to whats new page. Alport's syndrome One in a series of patient-oriented fact sheets produced by the Australian Kidney Foundation. This fact sheet focuses on Alport's syndrome (a genetic disease that causes progressive kidney damage), published in April 2001. Issues covered include the genetics of Alport's, common clinical signs and symptoms, diagnosis, treatment, and current research areas. This 2 page document is in PDF, which requires Adobe Acrobat Reader.
Last modified 21/Jun/2002 [Low Graphics]

85. MediFocus MedCenter Preview For Alport's Syndrome
MediFocus MedCenter © alport's syndrome (NK001) Introduction Nephritis issuesWhat are the most common symptoms of alport's syndrome?
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MediFocus MedCenter
Alport's Syndrome
Introduction
Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
AS affects the basement membranes which are the supporting layers of epithelial and endothelial tissues that make up much of the body's surfaces. The cause is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people.
Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
The cause of AS is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people. Treatment requires medication, and often, kidney transplant.

86. Alport's Syndrome
MediFocus™ Guide alport's syndrome. 15. The Medifocus Guide on alport's syndromeprovides answers to the following important questions and medical issues
http://www.yourbargainsite.com/med/Alports_Syndrome.html
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Alport's Syndrome
The Medifocus Guide on Alport's Syndrome
provides answers to the following important questions and medical issues:
  • What are the most common symptoms of Alport's Syndrome? Are there any recognized risk factors for developing Alport's Syndrome? What kinds of medical tests are used to establish the diagnosis of Alport's Syndrome? What is the current standard of care for the treatment of Alport's Syndrome? What treatment options are available for the management of Alport's Syndrome? Are there any promising new developments or potential breakthroughs in treatment? Who are the most notable medical authorities who specialize in Alport's Syndrome? Where are the leading hospitals and centers of research for Alport's Syndrome? What are the most important questions to ask my doctor about Alport's Syndrome?
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87. Reactions: Allison's Alport's Report
alport's syndrome is a genetic dysfunction in the kidney. alport's syndromeprimarily affects the glomerular membrane and makes it thin and weak.
http://www.johnfmartin.net/reaction/allison.htm
Alport's Health Report
By Allison McClelland Alport's Syndrome is a genetic dysfunction in the kidney. This syndrome is generally recognized as a common form of the disease Hereditary Nephritis. All the syndromes labeled under Hereditary Nephritis are brought about by a genetic dysfunction in the kidney and cause the kidney to wear and break down over time. There are many hereditary kidney diseases: Fabry Disease, Nail Patella Syndrome, Oxalosis, Hyperoxaluria and polycystic chronic hepatic fibrosis are a few of them. The kidney is a vital organ in the body that functions in the excretory system. The kidneys filter waste products from the blood and help to keep the body's balance of fluid and minerals. This is how urine is formed. The kidneys work as a filtration system that stops poison and diseases from building up in the blood. The position of the kidneys (one on each side of the backbone, near the back and right beneath the diaphragm,) make them very vulnerable to problems and injuries. Most of the problems, however, are caused by disease. Alport's Syndrome primarily affects the glomerular membrane and makes it thin and weak. Over time, Alport's can result in partial or full loss of kidney function; this is also referred to as acute renal failure. The symptoms of Alport's are noticeable blood and/or protein (chronic hematuria) in the urine causing the urine to turn orange, bright yellow, or even in some cases, red. In advanced levels of Alport's, uremia, hearing loss, vision problems or blindness may occur. A patient usually develops high blood pressure as the kidney function dissipates and will need to take medication to control the problem. Even with its many problems, the kidney may look pretty regular, although cysts may occur. Other symptoms of kidney problems are nausea, problems digesting food, sleepiness, skin becoming dry and icy, bruising easily, and loss of appetite.

88. Alport's Syndrome: MediFocus MedCenter Preview For Alport's Syndrome
alport's syndrome (NK001) Introduction The Medifocus Guide on alport's syndromeprovides answers to the following important questions and medical issues
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Introduction Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40. AS affects the basement membranes which are the supporting layers of epithelial and endothelial tissues that make up much of the body's surfaces. The cause is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people.

89. Alport's Syndrome Information Page Diseases Database
alport's syndrome Information Page. alport's syndrome related topics and differentials, Goalport'ssyndrome specific sites. GoSend alport's syndrome
http://www.diseasesdatabase.com/sieve/item1.asp?glngUserChoice=454

90. Alport's Syndrome
alport's syndrome. alport's syndrome Kidney Foundation of alportsyndrome Home Page - KEYWORDS alport or alport's syndrome
http://www.health-nexus.org/alport's_syndrome.htm
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Alport's Syndrome
Alport's Syndrome - Kidney Foundation of Canada General overview of the disease includes details on the genetics, symptoms, detection and treatment of this renal affliction.
Alport Syndrome Home Page ... KEYWORDS: Alport or Alport's syndrome, basement membranes, COL4A3, COL4A4, COL4A5and COL4A6 genes, collagen, deafness, dialysis, end-stage renal disease (ESRD ...
Alport's Syndrome
Alport's Syndrome: MediFocus MedCenter Preview for Alport's Syndrome Alport's Syndrome: MediFocus MedCenter Preview for Alport's Syndrome ... B Hepatitis C Lyme Disease Shingles Nephrology Alport's Syndrome Hypertension Polycystic Kidney Disease Renal Calculi ...
Alport's Syndrome The Medifocus Guide on Alports Syndrome provides answers to the following important questions and medical issues: What are the most common symptoms of Alport's Syndrome? Are there any recognized risk factors for developing Alports Syndrome?

91. HONselect - Nephritis, Hereditary
English Nephritis, Hereditary, alport's syndrome - Nephritis, Familial - alportsyndrome - alports syndrome - Familial Nephritides - Familial Nephritis.
http://www.hon.ch/HONselect/RareDiseases/C12.740.700.742.html
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English: Nephritis, Hereditary - Alport's Syndrome
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Français: ALPORT, SYNDROME - NEPHRITE HEMATURIQUE FAMILIALE AVEC SURDITE - NEPHROPATHIE FAMILIALE AVEC SURDITE Deutsch: Nephritis, hereditäre - Alport-Syndrom - Nephritis, familiäre - Nephropathie-Taubheits-Syndrom, hereditäres Español: NEFRITIS HEREDITARIA - SINDROME DE ALPORT - NEFRITIS FAMILIAR Português: NEFRITE HEREDITARIA - SINDROME DE ALPORT - NEFRITE FAMILIAR HONselect ressources Definition: Yes Articles: Yes Images: No News: No Conferences: No Clinical trials: No Web sites: English Yes Français No Deutsch Yes Español No Português No Home About us Site map Feedback ... HONewsletter http://www.hon.ch/HONselect/RareDiseases/C12.740.700.742.html Last modified: Thu Jul 25 2002

92. Alport's Syndrome - General Practice Notebook
alport's syndrome. alport's syndrome is a hereditary disease of basement membraneswhich is characterised by sensorineural deafness and renal failure.
http://www.gpnotebook.co.uk/cache/-898957312.htm
Alport's syndrome Alport's syndrome is a hereditary disease of basement membranes which is characterised by sensorineural deafness and renal failure. Inheritance can be X-linked dominant, autosomal dominant and, rarely, autosomal recessive. More information about the genetics of this condition is available in the linked menu item. Prevalence is about 1:5000. Pathological renal changes in Alport's syndrome include thickening of the glomerular basement membrane and splitting of the lamina densa.
Click here for more information...

93. Alports Syndrome
MediFocus MedCenter © alport's syndrome (NK001). Order the Full Guide.Introduction. What are the most common symptoms of alport's syndrome?
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Introduction
Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
AS affects the basement membranes which are the supporting layers of epithelial and endothelial tissues that make up much of the body's surfaces. The cause is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people.
Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.

94. Alport's Syndrome
alport's syndrome,, Print this article, (Arthur alport, 1880–1959, English physician),nephropathy, high tone sensineuronal deafness and ocular abnormality.
http://www.amershamhealth.com/medcyclopaedia/Volume VII/ALPORTS SYNDROME.asp
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*For Medical Professionals only, registration required Alport's syndrome, (Arthur Alport, 1880–1959, English physician), nephropathy, high tone sensineuronal deafness and ocular abnormality. The radiological findings are those of renal failure with loss of corticomedullary differentiation and renal enlargement which may progress to a small contracted kidney and renal cortical calcification. Also, see Alports syndrome kidney
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95. Alport's Syndrome, Kidney
alport's syndrome, kidney,, Print this article, (Arthur alport, 1880–1959,English physician), a syndrome consisting of hereditary
http://www.amershamhealth.com/medcyclopaedia/Volume IV 2/ALPORTS SYNDROME KIDNEY
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*For Medical Professionals only, registration required Alport's syndrome, kidney, (Arthur Alport, 1880–1959, English physician), a syndrome consisting of hereditary chronic nephritis, deafness and ocular abnormalities. Inheritance is usually autosomal dominant. Both sexes are affected, but the disease starts earlier in males and has a more rapid course. Clinical features include intermittent haematuria, progressive renal failure, and progressive high-frequency nerve deafness. Nephrotic syndrome is rare. Ocular abnormalities include posterior cataracts, lens dislocation, corneal dystrophy, nystagmus and myopia. Pathologically, the kidneys are small with patchy interstitial fibrosis. Foam cells in the vicinity of the corticomedullary junction are a distinctive microscopic finding. Intravenous urography or CT show small kidneys with impaired contrast excretion. Nephrocalcinosis may be present.
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96. MediFocus MedCenter Preview For Alport's Syndrome
MediFocus MedCenter ® Back to Directory alport's syndrome (NK001) Introduction Whatare the most common symptoms of alport's syndrome?
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Alport's Syndrome
Introduction
Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
AS affects the basement membranes which are the supporting layers of epithelial and endothelial tissues that make up much of the body's surfaces. The cause is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people.
Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
The cause of AS is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people. Treatment requires medication, and often, kidney transplant.

97. Entrez-PubMed
here to read Angiotensin converting enzyme inhibitor therapy in children with Alportsyndrome effect on urinary albumin, TGF beta;, and nitrite excretion.
http://www.biomedcentral.com/pubmed/11869456
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BMC Nephrol 2002;3(1):2 Related Articles, Links
Adler L, Mathew R, Futterweit S, Frank R, Gauthier BG, Kashtan CE, Trachtman H MD. Department of Pediatrics, Division of Nephrology, Schneider Children's Hospital of the North Shore-Long Island Jewish Health System, Long Island Campus for the Albert Einstein College of Medicine, New Hyde Park, NY and. trachtma@lij.edu PMID: 11869456 [PubMed - as supplied by publisher]
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