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Turner Syndrome: more books (74)

Parsonage-Turner syndrome: An entry from Thomson Gale's Gale Encyclopedia of Neurological Disorders by Greiciane Paneto, Iuri Louro, 2005
Group issues new turner syndrome guidelines.(News)(Disease/Disorder overview): An article from: Pediatric News by Christine Kilgore, 2007-02-01
Turner syndrome: An entry from Thomson Gale's Gale Encyclopedia of Science, 3rd ed. by Bryan Cobb, 2004
Le syndrome de Turner (French Edition) by Catherine Pienkowski, Maithé Tauber, 2009-03-13
New Turner syndrome guidelines urge better adult care.(Metabolic Disorders): An article from: Family Practice News by Christine Kilgore, 2007-02-15
Turner syndrome: An entry from Thomson Gale's Gale Encyclopedia of Children's Health: Infancy through Adolescence by Judith, MS Sims, L., MD, PhD, DrPH Fallon, 2006
Transition to adult care in Turner's, Klinefelter's. (Patients Fall Through Health Care Cracks).: An article from: Internal Medicine News by Erik L. Goldman, 2002-08-15
Early Tx prevents height loss in Turner's girls.(Clinical Rounds)(growth hormones ): An article from: Pediatric News by Michele G. Sullivan, 2005-02-01
Hearing, not height, troubles Turner's women.(Clinical Rounds): An article from: Pediatric News by Michele G. Sullivan, 2005-02-01
Maladie Chromosomique: Syndrome de Down, Syndrome 47,xyy, Syndrome de Klinefelter, Syndrome de Turner, Trisomie, Aneuploïdie (French Edition)
Gale Encyclopedia of Alternative Medicine: Restless leg syndrome by Judith Turner, 2001-01-01
Restless leg syndrome: An entry from Thomson Gale's Gale Encyclopedia of Alternative Medicine by Judith Turner, 2001
Turner's syndrome in 115 Danish girls born between 1955 and 1966 (Medicine series) by Johannes Nielsen, 1981
Coping with Turners Syndrome: A Mother's View by Elizabeth Moore, 2006-04-30

lists with details

Stanford Psychiatry Neuroimaging Laboratory: Turner Syndrome
What is turner syndrome? HH.Turner first described turner syndrome in 1938 and the chromosomal basis of this syndrome was established in 1959 by Ford.
http://spnl.stanford.edu/disorders/turners.htm

Extractions: What is Turner syndrome? Turner syndrome (45,X) is a genetic disorder that occurs only in females and arises from partial or complete absence of the X chromosome. H.H.Turner first described Turner syndrome in 1938 and the chromosomal basis of this syndrome was established in 1959 by Ford. Turner syndrome occurs in 1 in 2500 female births. The physical phenotype of this syndrome includes: gonadal dysgenesis lack of pubertal maturation infertility short stature shield chest webbing of the neck coarctation of the aorta horseshoe kidney The neurocognitive profile of females with Turner syndrome includes: T he psychosocial profile of females with Turner syndrome includes: What causes Turner Syndrome? Turner syndrome is the only sex chromosome disorder in which complete absence of an X chromosome is compatible with life. The loss of one of the sex chromosomes in Turner syndrome probably occurs after the zygote has formed or just after the fusion of the gametes. It has been determined that approximately 50% of cases have a 45,X karyotype with the remainder having mosaic karyotypes. In addition, it has been found that in 70 to 80 % of the cases, the retained X is maternal in origin. Researchers have begun to speculate as to the possibility that genes are present on the X chromosome which are expressed differently depending on the parental origin of the X chromosome. The effects of genomic imprinting can be analyzed from the standpoint of physical and physiologic parameters in females with Turner syndrome.
Turner Syndrome
Internet links on turner syndrome. Elsewhere on the Web. turner syndrome. I am your Guide, From Mary Kugler, Your Guide to Rare / Orphan Diseases.
http://rarediseases.about.com/library/weekly/aa020803a.htm

Extractions: zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') About Rare / Orphan Diseases Home Essentials ... Rare cancers zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Is it a Rare Disease? Rare Diseases A - B Rare Diseases C - D Rare Diseases E - H ... Help zau(256,138,125,'el','http://z.about.com/0/ip/417/0.htm','');w(xb+xb); Subscribe to the About Rare / Orphan Diseases newsletter. zau(256,152,100,'hs','http://z.about.com/5/ad/hs.htm?zIhsid=00',''); Search Rare / Orphan Diseases Email to a friend Print this page Stay Current Subscribe to the About Rare / Orphan Diseases newsletter. Suggested Reading Internet links on Turner syndrome Elsewhere on the Web Turner Syndrome Society of the United States Most Popular ALD and Lorenzo's Oil The Elephant Man's Bones Reveal Mystery Prune Belly (Eagle-Barrett) Syndrome Progeria Syndromes ... Mad Cow Disease and Humans What's Hot Autoimmune Kidney Disease Tourette Syndrome Christmas Disease Bugs, PANDAS, and Tics ... Dystonia and Botox Injections From Mary Kugler
National Library Of Medicine
Offers synonyms for turner syndrome, a summary and a list of major features.
http://www.nlm.nih.gov/cgi/jablonski/syndrome_cgi?term=Turner syndrome (TS)&
Turner Syndrome
turner syndrome. Rare/Orphan Diseases Blog. turner syndrome This inherited genetic disorder results from a missing or defective X (female) chromosome.
http://rarediseases.about.com/b/a/071531.htm

Extractions: zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') About Rare / Orphan Diseases Home Essentials ... Rare cancers zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Is it a Rare Disease? Rare Diseases A - B Rare Diseases C - D Rare Diseases E - H ... Help zau(256,138,125,'el','http://z.about.com/0/ip/417/0.htm','');w(xb+xb); Subscribe to the About Rare / Orphan Diseases newsletter. zau(256,152,100,'hs','http://z.about.com/5/ad/hs.htm?zIhsid=00',''); Search Rare / Orphan Diseases Rare/Orphan Diseases Blog Main Turner Syndrome
Pediatric Database
A definition of turner syndrome, followed by the epidemiology, pathogenesis, clinical features, investigations and management.
http://www.icondata.com/health/pedbase/files/TURNERSY.HTM
UAB Health System | Turner Syndrome
What is turner syndrome? turner syndrome is a genetic disorder a single X chromosome) was identified. What causes turner syndrome?
http://www.health.uab.edu/show.asp?durki=67115
Turner Syndrome Project
turner syndrome. Team members. Professor David Skuse (Head of Project) Kate Elgar Elena Morris. turner syndrome. Affects approximately
http://www.ich.ucl.ac.uk/units/bsunew/turner.htm
Turner Page
turner syndrome Page. Here is our history about Natascha, and here you will find links to other pages about turner syndrome. turner syndrome Society Texas.
http://home6.inet.tele.dk/justin/exploreTS.htm

Extractions: Turner Syndrome Page Here is our history about Natascha, and here you will find links to other pages about Turner Syndrome. Natascha was born at the last day of November 1996, already at birth we could see that something was wrong, but no one told us anything, until the third day, a doctor told us that she might have Turner Syndrome, but they had to do some test, Bloodtest to look after chromosones abnormalties, X-ray her kidneys, and there was this dissonace at her heart, so they had to scan her. all these examinations were done by the next couple of days, and the results from the bloodtest came at last, and they said " She is a Turner girl " our whole world fell apart that day, because we also knew that she had to go through an heart operation, in a age of 3 months, so we have to go and worry about this operation for 3 months, and the doctors told us a lot about turner Syndrome, and we got really scared because all that that could happen to our little babygirl.
Turner Syndrome
.turner syndrome. turner syndrome is a chromosomal disorder affecting females wherein one of the two Xchromosomes is defective or completely absent.
http://www.ehendrick.org/healthy/001413.htm

Extractions: Resources Turner syndrome is a chromosomal disorder affecting females wherein one of the two X-chromosomes is defective or completely absent. Chromosomes are structures in the nucleus of every cell in the human body. Chromosomes contain the genetic information necessary to direct the growth and normal functioning of all cells and systems of the body. A normal individual has a total of 46 chromosomes in each cell, two of which are responsible for determining gender. Normally, females have two X-chromosomes and males have one X and one Y-chromosome. In Turner syndrome, an error occurring very early in development results in an abnormal number and arrangement of chromosomes. Most commonly, an individual with Turner syndrome will be born with 45 chromosomes in each cell rather than 46. The missing chromosome is an X-chromosome. The affected person is always female. The prevalence of Turner syndrome is widely reported as being approximately one per 2,000 live female births, although researchers have reported prevalence rates that range from one in 3,125 to one in 5,000 live female births. About 1% to 2% of all female conceptions have a missing X-chromosome. Of these, the majority (99%) spontaneously abort, usually during the first trimester of
Turner Syndrome - Information / Diagnosis / Treatment / Prevention
home genetic disorders turner syndrome turner syndrome. NORD turner syndrome Offers alternative names, a general discussion and further resources.
http://www.healthcyclopedia.com/genetic-disorders/turner-syndrome.html
Turner Syndrome, Cincinnati Children's Hospital Medical Center
turner syndrome genetic abnormalities, features and heart defects information from the Heart Encyclopedia by the Heart Center staff at Cincinnati Children s
http://www.cincinnatichildrens.org/health/heart-encyclopedia/disease/syndrome/tu

Extractions: Home Contact Us Site Map Go to Advanced Search ... Heart-Related Syndromes Turner Syndrome Noonan Syndrome Down Syndrome Marfan Syndrome Velo-Cardio-Facial Syndrome ... Contact Us Genetic Abnormality, Features, Heart Defects Explanation Genetic Abnormality Prominent Features Heart Defects Turner syndrome was initially described by Dr. Henry Turner in 1938. Turner syndrome occurs in approximately 1 of 2,500 females. About 95 percent of fetuses are spontaneously miscarried during pregnancy and thus only 5 percent survive to term. Most cases of Turner syndrome occur randomly and thus do not carry a recurrence risk. Prenatal diagnosis is available through amniocentesis (sampling of the fluid which surrounds the baby before birth) to look for the abnormality of the X chromosome. Since patients with Turner syndrome are unable to have children, there is no risk of mother-daughter transmission. Return to Top Turner syndrome is characterized by an abnormality in the X chromosome. Normally females have two X chromosomes (and males have one X and one Y). In Turner syndrome, females often have only a single X chromosome. (This occurs in 60 percent of patients with Turner syndrome.)
Turner Syndrome: Keep Kids Healthy Conditions
turner syndrome, a chromosomal disorder that can cause girls to have short stature, a failure to begin puberty and infertility. turner syndrome.
http://www.keepkidshealthy.com/welcome/conditions/turner_syndrome.html

Extractions: Main Diseases and Conditions Turner syndrome is a chromosomal disorder that can cause girls to have short stature , a failure to begin puberty and infertility. Children with Turner syndrome only have one functioning X chromosome (unlike normal females who have two functioning X chromosomes [46, X, X]), and the other one may be absent [45, X] in all cells, or just some cells which is called a mosaic [45, X/46, X, X], or there may be a fragment of the second X chromosome present in some cells. It is not known what causes Turner syndrome and it is not associated with advanced maternal age. Turner syndrome is found in about 1 out of every 2000-3000 live born females.
UMHS Your Child Turner Syndrome (PWS)
Take our online survey. Type in a topic and hit the go button. turner syndrome. What is turner syndrome, and what do I need to know about testing and treatment?
http://www.med.umich.edu/1libr/yourchild/turners.htm

Extractions: Turner Syndrome What is Turner syndrome, and what do I need to know about testing and treatment? Turner syndrome is a genetic condition that occurs in females who have only one X chromosome, instead of the usual two. Typical features include short stature (height); webbed neck; underdeveloped breasts; abnormalities of the eyes and bones; and not getting your period (no menstruation). To learn more about genetics and to better understand how genes cause syndromes, see Your Child: Genetic Syndromes If your daughter has the physical features of Turner syndrome, then she should be tested to find out for sure whether she has it. A blood test can be done to check for the absence of an X chromosome.
Turner Syndrome
turner syndrome. turner syndrome is a disorder of the chromosomes affecting females, where one of the two X chromosomes is partially or completely absent.
http://www.chclibrary.org/micromed/00069390.html

Extractions: Chromosomes are structures in the nucleus of every cell in the body. Chromosomes contain the genetic information necessary to direct the growth and functioning of all the cells and systems of the body. A normal person has a total of 46 chromosomes in each cell, two of which are responsible for determining the sex of that person. Normally, females have two X chromosomes and males have one X and one Y chromosome. In Turner syndrome, an error very early in development results in an abnormal number and arrangement of chromosomes. Most commonly, a patient with Turner syndrome will be born with 45 chromosomes in each cell rather than 46. The missing chromosome is an X chromosome. About 1 in every 8,000 babies born has Turner syndrome. No cause has been identified for Turner syndrome. At birth, female babies with Turner syndrome are below average in weight and length. They have slightly swollen hands and feet, and sometimes have swelling at the nape of the neck. Girls with Turner syndrome are shorter than normal, and have short, webbed necks with extra, loose skin. The jaw is usually small and the ears are large. An extra fold of skin is often seen on either side of the nose, close to the eye (called an epicanthic fold). The chest is usually quite broad, with increased distance between the nipples.
Turner Syndrome - Lucile Packard Children's Hospital
HighRisk Newborn. turner syndrome What are monosomies? The term monosomy is turner syndrome. What is turner syndrome? turner syndrome
http://www.lpch.org/DiseaseHealthInfo/HealthLibrary/hrnewborn/turner.html

Extractions: What are monosomies? The term "monosomy" is used to describe the absence of one member of a pair of chromosomes. Therefore, there is a total of 45 chromosomes in each cell of the body, rather than 46. For example, if a baby is born with only one X sex chromosome, rather than the usual pair (either two Xs or one X and one Y sex chromosome), the baby would be said to have "monosomy X." Monosomy X is also known as Turner syndrome. What is Turner syndrome? Turner syndrome is a genetic disorder seen in girls that causes them to be shorter than others and to not mature sexually as they grow into adulthood. The severity of these problems varies among affected individuals. Other health problems may also be present involving the heart or renal system (i.e., kidneys). Many problems affecting girls with Turner syndrome can be managed or corrected with appropriate medical treatment. Turner syndrome occurs in one in 2,500 females born. The name "Turner syndrome" comes from Dr. Henry Turner, the physician who first described the collection of findings in 1938. It was not until 1959 that the cause of Turner syndrome (having only a single X chromosome) was identified.
Turner Syndrome - Lucile Packard Children's Hospital
Medical Genetics. turner syndrome What are monosomies? The term monosomy is turner syndrome. What is turner syndrome? turner syndrome
http://www.lpch.org/DiseaseHealthInfo/HealthLibrary/genetics/turner.html

Extractions: What are monosomies? The term monosomy is used to describe the absence of one member of a pair of chromosomes. Therefore, there is a total of 45 chromosomes in each cell of the body, rather than 46. For example, if a baby is born with only one X sex chromosome, rather than the usual pair (either two Xs or one X and one Y sex chromosome), the baby would be said to have "monosomy X." Monosomy X is also known as Turner syndrome. What is Turner syndrome? Turner syndrome is a genetic disorder seen in girls that causes them to be shorter than others and to not mature sexually as they grow into adulthood. The severity of these problems varies among affected individuals. Other health problems may also be present involving the heart or renal system (i.e., kidneys). Many problems affecting girls with Turner syndrome can be managed or corrected with appropriate medical treatment. Turner syndrome occurs in one in 2,500 females born. The name "Turner syndrome" comes from Dr. Henry Turner, the physician who first described the collection of findings in 1938. It was not until 1959 that the cause of Turner syndrome (having only a single X chromosome) was identified.
AllRefer Health - Turner Syndrome (Bonnevie-Ullrich Syndrome, Gonadal Dysgenesis
turner syndrome (BonnevieUllrich Syndrome, Gonadal Dysgenesis, Monosomy X) information center covers causes, prevention, symptoms, diagnosis, treatment
http://health.allrefer.com/health/turner-syndrome-info.html

Extractions: AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Pectus Excavatum A person's sex is determined by two chromosomes, the X and the Y. Usually, men have an X and a Y, while women have two X's. In Turner syndrome, a baby girl develops with only one X chromosome. The incidence is 1 out of 3,000 live births. Turner syndrome usually occurs sporadically, which means that the mutation occurs in fetal development and is not inherited from either parent. In rare cases, a parent silently carries rearranged chromosomes that can result in Turner syndrome in a daughter; this is the only situation in which Turner syndrome is inherited.
American Pregnancy Association - Birth Defects & Disorders: Turner Syndrome
turner syndrome. It is one of the most common chromosomal conditions occurring in about 1 out of every 2,500 live female births. What causes turner syndrome?
http://www.americanpregnancy.org/birthdefects/turnersyndrome.html

Extractions: Turner syndrome is a chromosomal condition that occurs when one of the two X chromosomes found in females is missing or incomplete. It is a chromosomal condition that only affects females. It is one of the most common chromosomal conditions occurring in about 1 out of every 2,500 live female births. Turner syndrome is caused by the complete or partial absence of one of the two X chromosomes normally found in a woman. There are no know reasons for the complete or partial absence of one of the X chromosomes and the condition appears to occur randomly. Turner syndrome is diagnosed using a blood test known as a karyotype. The karyotype blood test analyzes the chromosomal composition of the individual and determines whether the X chromosome is absent. A shorter stature and lack of ovarian development are the most common characteristics. A woman with Turner syndrome may exhibit any of the following physical characteristics: Are there any health concerns for someone with Turner Syndrome?
Turner Syndrome
turner syndrome Important It is possible that the main title of the report turner syndrome is not the name you expected. Please
http://my.webmd.com/hw/raising_a_family/nord112.asp

Extractions: Turner Syndrome is a rare chromosomal disorder of females characterized by short stature and the lack of sexual development at puberty. Other physical features may include a webbed neck, heart defects, kidney abnormalities, and/or various other malformations. Normally, females have two X chromosomes. In some cases of Turner Syndrome, however, one X chromosome is missing from the cells (45,X); research studies suggest that approximately 40 percent of these individuals may have some Y chromosomal material in addition to the one X chromosome. In other affected females, both X chromosomes may be present, but one may have genetic defects. In still other cases, some cells may have the normal pair of X chromosomes while other cells do not (45,X/46,XX mosaicism). Although the exact cause of Turner Syndrome is not known, it is believed that the disorder may result from an error during the division (meiosis) of a parent's sex cells.
Clinical Trial: Turner Syndrome: Genotype And Phenotype
turner syndrome Genotype and Phenotype. Adult women with turner syndrome have an increased risk of high blood pressure, diabetes mellitus and osteoporosis.
http://www.clinicaltrials.gov/ct/gui/show/NCT00006334?order=3

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