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         Down Syndrome Genetic Disorder:     more books (24)
  1. Down Syndrome: Visions for the 21st Century
  2. Advances in Down Syndrome Research
  3. The Down Syndrome Nutrition Handbook: A Guide to Promoting Healthy Lifestyles (Topics in Down Syndrome) by Joan E. Guthrie Medlen, 2002-11
  4. Down Syndrome: the Facts by Mark Selikowitz, 1997-01-15
  5. Genetic Disorders Sourcebook: Basic Consumer Health Information About Hereditary Diseases and Disorders, Including Cystic Fibrosis, Down Syndrome, Hemophilia, ... Disease (Health Reference Series)
  6. Protein Expression in Down Syndrome Brain (Journal of Neural Transmission Supplementum)
  7. Down Syndrome Behind the Dykes: Research in the Netherlands
  8. HECTOR'S INHERITANCE by Horatio Alger, 2010-02-12
  9. Hector's Inheritance - Horatio Alger by Horatio Alger, 2010-01-28
  10. Hector's Inheritance - Horatio Alger, JR. by JR. Horatio Alger, 2010-01-28

21. Facial Flushing Caused By Carcinoid Syndrome
Cushing's Syndrome Part of the Endocrine Resource Center From the Down Syndrome What Is Down Syndrome - Genetic Disorder Video - About.com
http://dermatology.about.com/od/facialflushing/a/ffcarcinoid.htm
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    Facial Flushing Caused by Carcinoid Syndrome
    From Heather Brannon, MD , former About.com Guide Updated July 02, 2008 About.com Health's Disease and Condition content is reviewed by the Medical Review Board
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    zSB(3,3) Carcinoid syndrome is a group of signs and symptoms that are associated with tumors of the enterochromaffin cells. These cells produce specific chemicals like serotonin, substance P, neuropeptide K, and neurokinin A. Enterochromaffin cells can be found in the intestines, appendix, rectum, lungs, stomach, pancreas, and thyroid. The carcinoid syndrome causes facial flushing, diarrhea and heart valve abnormalities. How Carcinoid Syndrome Causes Facial Flushing
    The facial flushing caused by carcinoid syndrome varies with the location of the tumor. The most common flush occurs in the head and neck area in response to excitement, exercise, drinking alcohol, and eating. It usually lasts only minutes. The flushing is caused by the sudden release of the chemicals produced by the enterochromaffin cells. Carcinoid syndrome is diagnosed by a specialized urine test that measures a chemical called 5-HIAA. Treatment of Facial Flushing With Carcinoid Syndrome
    The facial flushing of carcinoid syndrome is treated by removal of the tumor and administering a medication called

    22. Nucleus
    Journey into the Cell The Nucleus; Animal Cells; Down Syndrome What Is Down Syndrome - Genetic Disorder Video - About.com; Bacterial Reproduction
    http://biology.about.com/od/geneticsglossary/g/Nucleus.htm
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    Nucleus
    By Regina Bailey , About.com Guide
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    Nucleus The Virtual Cell zSB(3,3) Definition: The nucleus is a membrane bound structure that contains the cell's hereditary information and controls the cell's growth and reproduction. It is commonly the most prominent organelle in the cell The nucleus is surrounded by a structure called the nuclear envelope. This membrane separates the contents of the nucleus from the cytoplasm . The cell's chromosomes are also housed within the nucleus. Chromosomes contain DNA which provides the genetic information necessary for the production of other cell components and for the reproduction of life.
    Related Terms:
    genes mitochondria mitosis Cell Anatomy Cell Division Related Articles

    23. Understanding Klinefelter Syndrome
    Down Syndrome What Is Down Syndrome - Genetic Disorder Video - About.com; Male Body Waxing- Ask Male Body Waxing Expert, Loretta Wilson, Interview
    http://pediatrics.about.com/cs/conditions/a/klinefelter_syn.htm
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    A Guide for XXY Males and Their Families
    By Vincent Iannelli, M.D. , About.com Guide Updated March 18, 2007 About.com Health's Disease and Condition content is reviewed by the Medical Review Board Filed In:
  • Pediatrics
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    WHAT IS KLINEFELTER SYNDROME?
    In 1942, Dr. Harry Klinefelter and his coworkers at the Massachusetts General Hospital in Boston published a report about nine men who had enlarged breasts, sparse facial and body hair, small testes, and an inability to produce sperm. By the late 1950s, researchers discovered that men with Klinefelter syndrome, as this group of symptoms came to be called, had an extra sex chromosome, XXY instead of the usual male arrangement, XY. In the early 1970s, researchers around the world sought to identify males having the extra chromosome by screening large numbers of newborn babies. One of the largest of these studies, sponsored by the National Institute of Child Health and Human Development (NICHD), checked the chromosomes of more than 40,000 infants. Based on these studies, the XXY chromosome arrangement appears to be one of the most common genetic abnormalities known, occurring as frequently as 1 in 500 to 1 in 1,000 male births. Although the syndrome's cause, an extra sex chromosome, is widespread, the syndrome itself-the set of symptoms and characteristics that may result from having the extra chromosome-is uncommon. Many men live out their lives without ever even suspecting that they have an additional chromosome.

    24. Cockayne Syndrome
    Down Syndrome What Is Down Syndrome - Genetic Disorder Video - About.com; Top Warning Signs of Diabetes - Diabetes Symptoms - Symptoms of Diabetes
    http://rarediseases.about.com/cs/cockaynesyndrome/a/032203.htm
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    From Mary Kugler, R.N. , former About.com Guide Updated May 26, 2005 About.com Health's Disease and Condition content is reviewed by our Medical Review Board
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    zSB(3,3) What is it?
    Cockayne syndrome is an inherited disorder in which the genetic material (DNA) in body cells is damaged by ultraviolet radiation. Normally, the body can repair DNA damaged by sunlight, but people with Cockayne syndrome lack the ability to do that. What are the symptoms?
    There are two forms of Cockayne syndrome. The classic type, Type I, becomes apparent after the child is about a year old. Type II, or severe Cockayne syndrome, is apparent at birth. Because Cockayne syndrome affects many types of body cells, it affects many body systems. Some of its symptoms are:
    • pinched, narrow face and beaked nose

    25. Kearns Sayre Syndrome
    Down Syndrome What Is Down Syndrome - Genetic Disorder Video - About.com; Exercise-Induced Compartment Syndrome - Exertional Compartment Syndrome
    http://rarediseases.about.com/cs/kearnssayresynd/a/012404.htm
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    From Mary Kugler, R.N. , former About.com Guide Updated January 25, 2004 About.com Health's Disease and Condition content is reviewed by our Medical Review Board
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    zSB(3,3) Kearns Sayre syndrome is caused by problems with the genetic material in body cells. Specifically, it is due to defects in the DNA in mitochondria, the parts of cells that generate energy for the body to do its work. Kearns Sayre syndrome seems to occur sporadically (is not inherited). It affects people of all ethnic backgrounds. Symptoms
    There are three main features of Kearns Sayre syndrome:
    • It starts before age 20
    • Paralysis of certain eye muscles (external ophthalmoplegia) that gets worse over time
    • Degeneration of the retina, the part of the eye responsible for sight
    Because mitochondria are found in cells throughout the body, Kearns Sayre syndrome may affect many different organs and body systems. Symptoms may include:

    26. Klinefelter Syndrome 47,XXY
    Down Syndrome What Is Down Syndrome - Genetic Disorder Video - About.com; Turner Syndrome - Miscarriage Stillbirth and Monosomy X Turner Syndrome Dis
    http://breastcancer.about.com/od/types/p/klinefelter_syn.htm
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    By Pam Stephan , About.com Guide Updated January 19, 2007 About.com Health's Disease and Condition content is reviewed by the Medical Review Board
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    zSB(3,3) What is Klinefelter syndrome or 47,XXY?: Klinefelter syndrome is a rare genetic condition in which a man has an extra X chromosome. Some conditions associated with Klinefelter are hypothyroidism, infertility, testicular cancer, and an increased risk for male breast cancer. What are some symptoms?:
    • testosterone deficiency
    • enlarged breasts (gynecomastia)
    • sparse facial and body hair
    • small hard testes
    • inability to produce sperm (infertility)
    Chromosomes and Klinefelter syndrome, 47XXY: People typically have two sex chromosomes in each cell. Females have two X chromosomes, and males have one X and one Y. Males with Klinefelter syndrome most often have a single extra copy of the X chromosome, for a total of 47 chromosomes per cell; this is referred to as (47,XXY.) Some men with Klinefelter syndrome have the extra X chromosome in only some of their cells; this is called "mosaic 46,XY/47,XXY." Extra copies of the X chromosome interfere with male sexual development and testicular functioning, thus explaining some of the conditions outlined above.

    27. Cause Of Sjogren's Syndrome - What Causes Sjogren's Syndrome?
    Causes of Chronic Fatigue Syndrome Possible Causes of Chronic Fatigue Syn Down Syndrome - What Is Down Syndrome - Genetic Disorder Video - About.com
    http://arthritis.about.com/od/sjogrens/ss/sjogrens_4.htm
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    By Carol Eustice , About.com Guide Updated February 25, 2007 About.com Health's Disease and Condition content is reviewed by the Medical Review Board
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    Part 4 of 10 - What Causes Sjogren's Syndrome?
    Combination Of Factors?
    Researchers think Sjogren's syndrome is caused by a combination of genetic and environmental factors. Several different genes appear to be involved, but scientists are not certain exactly which ones are linked to the disease since different genes seem to play a role in different people. For example:
  • There is one gene that predisposes Caucasians to the disease. Other genes are linked to Sjogren's syndrome in people of Japanese, Chinese, and African American descent.
  • 28. Central Nervous System Disorders | PHP
    Down Syndrome; Genetic Disorder; Learning Disability; Mental Health Disorders; Intellectual Disability; Multiple Sclerosis; Muscular Dystrophy; Orthopedic Disabilities
    http://www.php.com/taxonomy/term/59?page=9

    29. Brad And Angelina Twins Down Syndrome Rumors - Do Brad And Angelina's Twins Have
    Children with the Down syndrome genetic disorder are detected by developmental delays physical characteristics, include rounded face, flattened profiles and upward slanted eyes.
    http://gossip.about.com/od/healthfitness/f/Brad_Angie_Twins_Down_Syndrome.htm
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    Do Brad and Angelina's Twins, Knox and Vivienne, Have Down Syndrome?
    By Diana Mimon , About.com Guide
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    Photo Credit: National Enquirer May 2010 zSB(3,3) Question: Do Brad and Angelina's Twins, Knox and Vivienne, Have Down Syndrome? Answer: May 2010 Rumors have been circulating on the internet that Brad Pitt and Angelina Jolie's twins, Knox and Vivienne, born in July 2008 , could have Down Syndrome. There is a feature article in the National Enquirer highlighting the fact that the rumors mills are suggesting that there may be some serious health issues for Brad and Angelina's famous twins. "Children with the Down syndrome genetic disorder are detected by developmental delays physical characteristics, include rounded face, flattened profiles and upward slanted eyes. And it's those descriptions that have sparked the false online speculation," according to the National Enquirer Could there actually be any truth to this latest round of gossip surrounding the Jolie-Pitt twins?

    30. Chromosome 21 News, Research
    Tags Alzheimer's Disease, Brain, Cell, Chromosome, Chromosome 21, Cognitive Function, Dementia, DNA, DNA Methylation, Down Syndrome, Genetic Disorder, Insulin, Insulin Resistance
    http://www.news-medical.net/?tag=/Chromosome 21

    31. Karyotype - What Is A Karyotype
    Down Syndrome What Is Down Syndrome - Genetic Disorder Video - About.com; Genetics Genealogy by Thomas H Roderick PhD - Virtual Lecture; Chromosome Karyotype or CMA Testing
    http://downsyndrome.about.com/od/downsyndromeglossary/g/karyotypedef_ro.htm
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    Karyotype
    From Kathleen Fergus , former About.com Guide Updated March 16, 2009 About.com Health's Disease and Condition content is reviewed by the Medical Review Board
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    A karyotype showing trisomy 21 Istockphoto/K. Fergus Definition: Down syndrome is diagnosed by a karyotype test. Pronunciation: Also Known As: chromosome test, chromosome analysis Examples: A karyotype showed that the baby had an extra number 21 chromosome and thus had 47 chromosomes instead of 46. How a Karyotype Test is Done Related Articles if(zSbL<1)zSbL=3;zSB(2);zSbL=0 Related Searches chromosome analysis chromosome abnormalities number of chromosomes karyotype ... microscope
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    32. Hyper-IgM Syndrome
    Down Syndrome What Is Down Syndrome - Genetic Disorder Video - About.com; Severe Combined Immunodeficiency; Receptors for Recognizing Antigen Understanding the Immune System, Inclu
    http://pediatrics.about.com/od/primaryimmunodeficiency/a/hyper_igm.htm
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    By Vincent Iannelli, M.D. , About.com Guide Updated October 30, 2004 About.com Health's Disease and Condition content is reviewed by the Medical Review Board
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  • Medical Advice Diseases and Conditions Primary Immunodeficiency
  • zSB(3,3) Hyper-IgM is a rare immunodeficiency disease in which the immune system fails to produce IgA and IgG antibodies.
    What causes hyper-IgM syndrome?
    A flawed gene (or genes) in T cells is responsible for hyper-IgM syndrome. The faulty T cells do not give B cells a signal they need to switch from making IgM to making IgA and IgG. Most cases of hyper-IgM syndrome are linked to the X chromosome. Because boys carry only one X chromosome, unlike girls whose second X chromosome helps to protect against the disease, more boys than girls have IgM syndrome.
    What are the symptoms of hyper-IgM syndrome?

    33. Maternal Age - Definition Of Maternal Age In The Medical Dictionary - By The Fre
    there are some abnormalities and labor complication that are tend to happened (statistically) along with the increase of mother's age (such as down syndrome, genetic disorder
    http://medical-dictionary.thefreedictionary.com/Maternal age

    34. Genetics: An Extra Pair Of Chromosones, Extra Chromosome, Liver Cells
    Found in Our DNA • Genetics amp; Genealogy by Thomas H Roderick PhD Virtual Lecture • Klinefelter syndrome 47,XXY • Down Syndrome - What Is Down Syndrome - Genetic Disorder
    http://en.allexperts.com/q/Genetics-1795/extra-pair-chromosones.htm
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    35. Down Syndrome News, Research
    Tags Alzheimer's Disease, Brain, Cell, Chromosome, Chromosome 21, Cognitive Function, Dementia, DNA, DNA Methylation, Down Syndrome, Genetic Disorder, Insulin, Insulin Resistance
    http://www.news-medical.net/?tag=/Down Syndrome

    36. Angelina Jolie & Brad Pitt’s Twins Have Down Syndrome?
    Children with the Down syndrome genetic disorder are detected by developmental delays physical characteristics, include rounded face, flattened profiles and upward slanted eyes.
    http://thebosh.com/archives/2010/05/angelina_jolie_brad_pitts_twins_have_down_sy
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      May 2, 2010
      Angelina Jolie Brad Pitt ’s Twins Have Down Syndrome? Online Chatter about BRAD PITT and ANGELINA JOLIE 's babies Knox and Vivienne is heartbreaking. According to National Enquirer , gossips claim BRAD PITT and ANGELINA JOLIE's 21-month-old twins are suffering from Down syndrome. Bloggers say the children appear to have the developmental disorder. Children with the Down syndrome genetic disorder are detected by developmental delays physical characteristics, include rounded face, flattened profiles and upward slanted eyes. According to The National Institute of Health , a 35-year-old woman has a 1 in 400 chance of having a child with DS, which means, mathematically, there is 0.000625 percent chance that both twins, with different DNA, would have DS reports Babble. ”They hate that their kids are under such intense observation. It’s very difficult for them to deal with. As far as their concerned, Knox and Vivienne are perfect. Brad and Angie aren’t the type to sweep sensitive issues under the carpet,” a friend of the couple says. “The twins are healthy, but if there were medical problems with them, I think Brad and Angie would subtly try to destigmatize the issue by not hiding them.”

    37. Obgyn — Blogs, Pictures, And More On WordPress
    Tags Living with Down syndrome, Down syndrome, Advocacy 2, Down Syndrome, genetic disorder, Conditions and Diseases, trisomy21, prenatel, abc
    http://en.wordpress.com/tag/obgyn/

    38. YouTube - Down Syndrome
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    http://www.youtube.com/watch?v=ycrPCTP2mFE

    39. Chromosome - What Is A Chromosome
    Down Syndrome What Is Down Syndrome - Genetic Disorder Video - About.com; Sex Chromosome Abnormalities; Genetic Basics - Understanding the Clues Found in Our DNA
    http://downsyndrome.about.com/od/downsyndromeglossary/g/chromosomedf_ro.htm
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    Chromosome
    From Kathleen Fergus , former About.com Guide Updated March 16, 2009 About.com Health's Disease and Condition content is reviewed by the Medical Review Board
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    Definition: Chromosome - packages of genetic information contained in every cell of the human body. Most people have 46 chromosomes. People with Down syndrome have 47 chromosomes. People with Down syndrome have an extra chromosome 21. Most people with Down syndrome have an entire extra #21 chromosome in every cell of their body - a condition called trisomy 21. People can also have Down syndrome as a result of an extra #21 in only some of their cells (called Mosaic Down syndrome ) or because two of their chromosomes are stuck together, a condition called a translocation. Pronunciation: "chrome" "o""sew""m" Examples: Down syndrome is caused by an extra chromosome number 21.

    40. MEDICAL TERMINOLOGY
    HIERARCHY CONT. CELL (CYTOLOGY; CELL BIOLOGY) NUCLEUS; CELL MEMBRANE (plasma membrane, phospholipid bilayer) CYTOPLASM (cytosol) MITOCHONDRIA (cellular respiration
    http://faculty.leeu.edu/~jboyer/hsc398/MED term cell bio and prefix.ppt

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