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         Polycystic Kidney:     more books (43)
  1. Medifocus Guidebook on: Polycystic Kidney Disease by Medifocus.com Inc., 2010-07-21
  2. The Official Patient's Sourcebook on Polycystic Kidney Disease
  3. Polycystic Kidney Disease (Oxford Clinical Nephrology Series)
  4. Autosomal Dominant Polycystic Kidney Desease: Seminar on Autosomal Dominant Polycystic Kidney Disease, Vimercate, June 18, 1994 (Contributions to Nephrology) by Seminar on Autosomal Dominant Polycystic Kidney Disease, A. Sessa, 1995-12
  5. Polycystic Kidney Disease (Contributions to Nephrology) by M. H. Breuning, M. Devoto, 1992-07
  6. ADPKD patients manual: Understanding and living with autosomal dominant polycystic kidney disease by Irene T Duley, 1995
  7. Problems in Diagnosis and Management of Polycystic Kidney Disease: Proceedings of the First International Workshop on Polycystic Kidney Disease
  8. The Cystic Kidney (Developments in Nephrology)
  9. Conquering Kidney Disease - Identifying Potential Problems by Merle Fields, 2010-05-31
  10. Health tips for living with polycystic kidney disease by Arlene B Chapman, 2001
  11. Polycystic kidney disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Paul Johnson, 2005
  12. ADVANCES IN THE PATHOGENESIS OF POLYCYSTIC KIDNEY DISEASE by F.; Dobbie, J.W. Carone, 1990
  13. PKD patient's manual: Understanding & living with autosomal dominant polycystic kidney disease by Irene Duley, 1989
  14. Polycystic Kidney Disease Medical Guide by Qontro Medical Guides, 2008-07-09

81. Autosomal Dominant Polycystic Kidney Disease (ADPKD)
Autosomal Dominant polycystic kidney Disease (ADPKD)
http://mayoresearch.mayo.edu/mayo/research/harris_lab/adpkd.cfm
Harris Lab (Polycystic Kidney Disease) Lab Home
current projects
Autosomal Dominant Polycystic Kidney Disease (ADPKD) Autosomal Recessive Polycystic Kidney Disease (ARPKD)
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AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE (ADPKD)
We are pursing two interrelated projects to understand the mutational mechanism and phenotypic consequences of mutation to PKD1. 1. Genotype/phenotype correlations Please click thumbnails for larger image. Figure 1-1. Structure of the PKD1 (top) and PKD2 (bottom) genes and the transcripts they encode. Mutation to either of these genes results in ADPKD. Figure 1-2. Many different types of mutation: splicing (light blue) frameshifting (dark blue) or in-frame (pink) insertions or deletions, missense (yellow) or nonsense (purple) to PKD1 cause ADPKD. Mutations are found throughout the gene. Figure 1-3. Intracranial aneurysms occur in a minority of ADPKD families. This diagram shows that mutations that effect the first part of polycystin-1 are more often associated with aneurysms than those to the end of the protein. 2. Characterization of mutant polycystin-1 products

82. Polycystic Kidney Disease (PKD) - January 1, 2005 - American Family Physician
polycystic kidney disease (also called PKD) tends to run in families. Sacs of fluid (called cysts) grow in the kidneys. They are like little water balloons.
http://www.aafp.org/afp/20050101/137ph.html

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Journals Vol. 71/No. 1 (January 1, 2005)
Please note: This information was as current as we could make it on the date given above. But medical information is always changing, and some information given here may be out of date. For regularly updated information on a variety of health topics, please visit familydoctor.org , the AAFP patient education Web site.
Patient Information Collection
kidney and urinary health Polycystic Kidney Disease (PKD) What do the kidneys do? Kidneys remove waste products from your blood. They do this by filtering the blood and making urine. The urine carries waste products out of your body. What is polycystic kidney disease? Polycystic kidney disease (also called PKD) tends to run in families. Sacs of fluid (called cysts) grow in the kidneys. They are like little water balloons. If too many cysts grow or if they get too big, the kidneys are damaged. The cysts may be painful or get infected. Children of persons with PKD have a 50 percent chance of getting the disease.

83. Polycystic Kidney Disease
Online health news and information for consumers.
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Polycystic Kidney Disease
Polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of numerous cysts in the kidneys. The Polycystic Kidney Disease Foundation (PKDF) calls PKD the most common genetic, life threatening disease, affecting more people than cystic fibrosis, muscular dystrophy, hemophilia, Down syndrome and sickle cell disease combined. (Read about " Cystic Fibrosis, " muscular dystrophy in " Neuromuscular Diseases, " hemophilia in " Bleeding Disorders, " " Down Syndrome " and " Sickle Cell Disease ") PKDF estimates over half a million people in the United States suffer with PKD. The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) calls it the fourth leading cause of kidney failure. (Read about kidney failure in " End Stage Renal Disease ") The cysts, which are filled with fluid, can slowly replace much of the mass of the kidneys, reducing kidney function and leading to kidney failure. When PKD causes kidneys to fail - which usually happens only after many years, according to NIDDK - the patient requires dialysis or kidney transplantation. PDKF says that over half of people with the major type of PKD progress to kidney failure, i.e. end-stage renal disease (ESRD). The kidneys are two organs, each about the size of a fist, located in the upper part of a person's abdomen, toward the back. The kidneys filter wastes from the blood to form urine. They also regulate amounts of certain vital substances in the body. (Read about "

84. Polycystic Kidney Disease - OhioHealth
polycystic kidney disease isn t limited just to your kidneys. Common complications include high blood pressure and kidney failure.
http://www.ohiohealth.com/healthreference/reference/821423B5-5A42-4E3D-B75593AEA

85. Polycystic Kidney Disease: Information From Answers.com
polycystic kidney Disease What is polycystic kidney Disease? polycystic kidney disease (PKD) is a disorder that is characterized by the growth of.
http://www.answers.com/topic/polycystic-kidney-disease-1
showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Diagnosis Wikipedia Mentioned In Or search: - The Web - Images - News - Blogs - Shopping polycystic kidney disease Diagnosis Polycystic Kidney Disease What is Polycystic Kidney Disease?
Polycystic kidney disease (PKD) is a disorder that is characterized by the growth of numerous cysts in the kidneys. The cysts are filled with fluid. PKD cysts can replace much of the mass of the kidneys, thereby reducing kidney function and leading to kidney failure The kidneys are two organs, each about the size of a fist, that are located in the upper part of the abdomen, towards the back. The kidneys filter wastes from the blood to form urine. They also regulate amounts of certain vital substances in the body. When PKD causes kidneys to fail, which usually happens only after many years, the patient requires dialysis or kidney transplantation. About one-half of people with the primary form of PKD progress to kidney failure or end-stage renal disease (ESRD). PKD can cause cysts in the liver and problems in other organs, such as the heart and blood vessels in the brain. These complications help doctors distinguish PKD from the usually harmless "simple" cysts that often form in the kidneys in later years of life.

86. Medifocus: Polycystic Kidney Disease Guidebook
polycystic kidney Disease Prognosis PKD Treatment Options.
http://www.medifocus.com/polycystic-kidney-disease.php?a=a

87. UpToDate Patient Information: Polycystic Kidney Disease
In polycystic kidney disease, the kidneys become enlarged with multiple cysts that There are two major forms of polycystic kidney disease autosomal
http://patients.uptodate.com/topic.asp?file=kidn_dis/6183

88. Polycystic Kidney Disease
polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of polycystic kidney Research Foundation 4901 Main Street Suite 320
http://www.duj.com/Polycystic.html
Polycystic Kidney Disease
Polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of
numerous cysts in the kidneys. The cysts are filled with fluid. PKD cysts can slowly replace
much of the mass of the kidneys, reducing kidney function and leading to kidney failure.
The kidneys are two organs, each about the size of a fist, located in the upper part of a
person's abdomen, toward the back. The kidneys filter wastes from the blood to form urine.
They also regulate amounts of certain vital substances in the body.
When PKD causes kidneys to failwhich usually happens only after many yearsthe patient
requires dialysis or kidney transplantation. About one-half of people with the major type of
PKD progress to kidney failure, i.e., end-stage renal disease (ESRD).
PKD can cause cysts in the liver and problems in other organs, such as the heart and blood vessels in the brain. These complications help doctors distinguish PKD from the usually harmless "simple" cysts that often form in the kidneys in later years of life. In the United States, about 500,000 people have PKD, and it is the fourth leading cause of

89. MyDNA.com - Polycystic Kidney Disorders
myDNA is a consumer focused health, genetics, and genomics information provider offering disease condition information, health wellness tips,
http://www.mydna.com/health/kidney/pkd
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90. Polycystic Kidney Disease Medical Reference - MedicineOnline.com
polycystic kidney disease is an inherited kidney disorder that enlarges the As many as 50% of people with polycystic kidney disease also have cysts on
http://www.medicineonline.com/reference/Diseases_and_Conditions/Renal_&_Reproduc
Medical References
  • Health Topics Medical Dictionary Drug Information Index ... Providers Login Search for Containing Exact Match The web References [ DISEASES AND CONDITIONS ] Polycystic kidney disease Diseases and Conditions Kidney Failure > Polycystic kidney disease Polycystic kidney disease Sections >>
    Illustrations

    Alternative names

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    Causes, incidence, and risk factors
    ...
    Calling your health care provider

    Illustrations
    Kidney and liver cysts - CT scan
    Liver and spleen cysts - CT scan
    Alternative names
    Cysts - kidneys; Kidney - polycystic; Autosomal dominant polycystic kidney disease; ADPKD
    Definition Polycystic kidney disease is an inherited kidney disorder that enlarges the kidneys and interferes with their function because of multiple cysts on the kidneys. Causes, incidence, and risk factors Polycystic kidney disease (PKD) is an inherited disorder (with autosomal dominant inheritance if one parent carries the gene, the children have a 50% chance of developing the disorder) where multiple clusters of cysts form on the kidneys. The exact mechanism that triggers
  • 91. Kidney Cysts
    polycystic kidney Disease National Kidney Foundation PDF File; polycystic kidney Disease Merck Manual, 2nd Home Edition
    http://www.noah-health.org/en/kidver/kidney/specific/cysts.html
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    Polycystic Kidney Disease

    92. Polycystic Kidney Disease
    polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of numerous cysts in the kidneys. The cysts are filled with fluid.
    http://members.shaw.ca/vanderwyst/PKD.html
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    WHAT IS PKD?
    Polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of numerous cysts in the kidneys. The cysts are filled with fluid. PKD cysts can slowly replace much of the mass of the kidneys, reducing kidney function and leading to kidney failure. PKD can cause cysts in the liver and problems in other organs, such as the heart and blood vessels in the brain. The most common symptoms are pain in the back and the sides (between the ribs and hips), and headaches. The dull pain can be temporary or persistent, mild or severe. People with autosomal dominant PKD also
    can experience the following:
    Urinary tract infections Hematuria (blood in the urine) Liver and pancreatic cysts Abnormal heart valves High blood pressure Kidney stones Brain Aneurysms (bulges in the walls of blood vessels) Diverticulosis (small sacs on the colon).

    93. Polycystic Kidney Of The Kidney
    polycystic kidney of Kidney From the Virtual Pathology Museum, Department of Pathology, University of Connecticut Health Center.
    http://radiology.uchc.edu/eAtlas/GU/529.htm
    Search Frames Search No frames PathWeb Home Feed Back ... About Infantile Polycystic Kidney
    Click on Image to Enlarge it Infantile Polycystic Kidney
    The cysts affect the renal parenchyma diffusely.
    Both the cortex and the medulla are affected.
    The cysts involving the cortex are not spherical, but tend to be elongate. They actually represent cystically dilated collecting ducts and tubules. (Description By:H. Yamase, M.D. ) (Image Contrib. by: UCHC ) Infantile Polycystic Kidney Disease Etiology
    Genetic, autosomal recessive. Pathogenesis
    The pelvis, calyces, papillae as well as the nephrons are believed to develop normally in the initial stages of renal genesis.
    The cystic development of the collecting ducts are believed to occur subsequently by a hyperplastic process., Epidemiology
    Developmental disorder of the kidneys discovered in developing fetuses (by ultrasound) or in the newborn period (enlarged kidneys). General Gross Description
    The kidneys are bilateral and symmetrically enlarged but retain a reniform shape.

    94. Polycystic Kidney Of The Kidney
    polycystic kidney of Kidney From the Virtual Pathology Museum, Department of Pathology, University of Connecticut Health Center.
    http://radiology.uchc.edu/eAtlas/GU/1568.htm
    Search Frames Search No frames PathWeb Home Feed Back ... About Infantile Polycystic Kidney Disease
    Click on Image to Enlarge it Infantile Polycystic Kidney Disease
    The photograph shows renal capsule at the top with a peripheral zone of recognizable immature nephronic elements.
    The cysts in the deeper parenchyma are obvious.
    Cysts in infantile polycystic kidney disease are derived from the collecting ducts. This is based on nephron microdissection and immunohistochemical staining. (Description By:H. Yamase, M.D. ) (Image Contrib. by: UCHC ) Infantile Polycystic Kidney Disease Etiology
    Genetic, autosomal recessive. Pathogenesis
    The pelvis, calyces, papillae as well as the nephrons are believed to develop normally in the initial stages of renal genesis.
    The cystic development of the collecting ducts are believed to occur subsequently by a hyperplastic process., Epidemiology
    Developmental disorder of the kidneys discovered in developing fetuses (by ultrasound) or in the newborn period (enlarged kidneys).

    95. Polycystic Kidney Disease
    Illustration of kidney system, polycystic kidney Disease polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of numerous
    http://www.medhelp.org/NIHlib/GF-340.html

    Polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of numerous cysts in the kidneys. The cysts are filled with fluid. PKD cysts can slowly replace much of the mass of the kidneys, reducing kidney function and leading to kidney failure. The kidneys are two organs, each about the size of a fist, located in the upper part of a person's abdomen, toward the back. The kidneys filter wastes from the blood to form urine. They also regulate amounts of certain vital substances in the body. When PKD causes kidneys to failwhich usually happens only after many yearsthe patient requires dialysis or kidney transplantation. About one-half of people with the major type of PKD progress to kidney failure, i.e., end-stage renal disease (ESRD). PKD can cause cysts in the liver and problems in other organs, such as the heart and blood vessels in the brain. These complications help doctors distinguish PKD from the usually harmless "simple" cysts that often form in the kidneys in later years of life. In the United States, about 500,000 people have PKD, and it is the fourth leading cause of kidney failure. Medical professionals describe two major inherited forms of PKD and a noninherited form:

    96. FamilyFun: Health Encyclopedia: Polycystic Kidney Disease
    An excerpt on polycystic kidney disease from the Disney Encyclopedia of Baby and Child Care.
    http://familyfun.go.com/parenting/child/health/childhealth/dony79enc_kidn/
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    ... Solutions A to Z Polycystic Kidney Disease
    This hereditary kidney disorder occurs in two main forms. The more common form, known as adult polycystic disease (APCD), usually develops in adulthood but may, in rare cases, manifest itself in infancy or childhood. Much less common is infantile polycystic disease (IPCD), which is usually apparent soon after birth and is accompanied by liver abnormalities. In both forms of the disease, the kidney is riddled with fluid-filled growths called cysts. These cysts, which usually appear in both kidneys, severely impair kidney functioning. In the infantile form of the disease, the kidneys may be either enlarged or underdeveloped. Some infants also are born with a noninherited cystic kidney disorder called multicystic kidney of the newborn. This disorder, which usually affects only one kidney, occurs when the ureter (the tube to the bladder) develops abnormally, causing the kidney to degenerate into an irregular mass of cysts. HOW DOES POLYCYSTIC KIDNEY DISEASE DEVELOP?

    97. The Feline PKD FAQ -- Answers To Frequently Asked Questions About PKD In Cats
    About polycystic kidney Disease in Cats faqsponsor.jpg (23967 bytes) PKD (polycystic kidney Disease) is a progressive, genetic disease of the kidneys.
    http://my.erinet.com/~lebordo/PKD/pkdfaq.html
    The Feline PKD FAQ
    Answers to Frequently Asked Questions
    About Polycystic Kidney Disease in Cats
    NOTE: In 2004, the University of California Davis developed a DNA test for PKD. It should be 100% accurate at any age.
    See the UC Davis Veterinary Genetics Lab web site for details Veterinary Diagnostics Center in Fairfield, Ohio has independently developed a DNA test for feline PKD. I participated in their testing by sending 4 samples, and the results were identical to previous scanned results (1 positive and 3 negatives). See the Veterinary Diagnostics Center web site for details. Last updated 7/1/2005. The following Frequently Asked Questions about PKD were last revised 5/30/2002. The genetic discussion should still be accurate. Information about diagnosis is obviously outdated, as noted above. Information on frequency, available treatments, outcome, etc., may or may not be current. T his FAQ is no longer being maintained, but is being preserved for reference purposes

    98. Polycystic Kidney Disease -- ECureMe.com
    UPDATED SARS INFORMATION,Check health symptoms, make a self diagnosis, ask a doctor or veterinarian online, view an encyclopedia of diseases treatments,
    http://www.ecureme.com/emyhealth/data/Polycystic_Kidney_Disease.asp
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    Polycystic Kidney Disease
    more about Polycystic Kidney Disease

    PKD, Multiple Renal Cysts , or Kidney Cysts
    • PKD is a disorder characterized by the development of multiple, balloon like sacs (cysts) in one or both kidneys. The cysts are filled mostly with fluid, but may contain semi-solid material. Over time (after many years), the cysts can replace most of the kidney and reduce its ability to remove the body's toxic wastes and reabsorb vital nutrients (i.e., renal or kidney failure).

    99. Polycystic Kidney Diseases
    The US PKD (polycystic kidney Research) Foundation was founded in 1982 and aims An illustrated patient information document on polycystic kidney disease
    http://omni.ac.uk/browse/mesh/D007690.html
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    Polycystic Kidney Diseases
    Polycystic Kidney Diseases Polycystic Kidney Diseases / pathology broader: Urogenital Abnormalities other: Bladder Exstrophy Cryptorchidism Epispadias Hypospadias ... Nephritis, Hereditary narrower: Polycystic Kidney, Autosomal Recessive
    Polycystic Kidney Diseases
    PKD Foundation The US PKD (Polycystic Kidney Research) Foundation was founded in 1982 and aims to determine the cause, improve clinical treatment and find a cure for polycystic kidney disease. The site provides details about the Foundation, as well as information for professionals and patients. The information provided includes research information, news, details of publications, and conferences as well as information on PKD. United States Polycystic Kidney Diseases Organizations, Nonprofit Charities ... Introduction to the kidneys and PKD An illustrated patient information document on polycystic kidney disease (PKD), from the Polycystic Kidney Research Foundation. Information is provided on what the kidneys do, what PKD is, what cysts are, the symptoms, complications, how it spreads, testing, and controlling the disease. A PKD glossary is also provided. Polycystic Kidney Diseases Patient Education Handout [Publication Type]
    Polycystic Kidney Diseases / pathology
    Pathology of renal cystic disease A collection of images with explanatory text forming an illustrated tutorial on the pathology of renal cystic disease. Includes recessive polycystic kidney disease (RPKD), multicystic renal dysplasia, dominant polycystic kidney disease (DPKD), cystic change with obstruction, and a section on miscellaneous cystic renal changes in adults. This tutorail is from the University of Utah's WebPath server.

    100. Dad's PKD Polycystic Kidney Disease, ADPKD.
    Steve and polycystic kidney Disease ADPKD- family fun and family health PKD,polycystic kidney disease,ADPKD I had known for a long time that I had PKD
    http://www.specialneedsfamilyfun.com/family/PKD-polycystic-kidney-disease.htm
    Steve and Polycystic Kidney Disease - ADPKD- family fun and family health information
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    Tour I had known for a long time that I had PKD (polycystic kidney disease.) I had inherited it from my mother Millie. My mother had died from a brain aneurysm (one of the symptoms of PKD) an hour after I was born. Almost more than anything, I wish I had a chance to know her.
    My father was devasted by my mother's death and mourned silently the rest of his life. I recently reviewed my mother's death certificate and realized that my parents had only been married for a year before she died. I have no siblings.
    Symptoms of my Polycystic Kidney Disease did not start to appear until I was 48 years old. I began to notice that I woke up with a pain in my abdomen every morning. I thought that this was just a belly ache, but after awhile I realized that the pain was from my enlarged kidneys.
    Since this is a genetic disease, I hope that my two daughters don't inherit this. To the left is a recent Christmas picture of my oldest daughter Monica and I. My sweetheart Monica is already dealing with enough from multiple handicaps not related to PKD.

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