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Topic: Trisomy 13


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 Trisomy 18 & 13 - Lucile Packard Children's Hospital
Families who have or have had a baby with trisomy 18 or trisomy 13 are particularly helpful and supportive since they have experienced many of the same questions and emotions.
Since trisomy 18 and trisomy 13 each have a unique group of characteristics, a physician may be able to determine simply by physical examination whether a baby has trisomy 18 or 13.
http://www.lpch.org/DiseaseHealthInfo/HealthLibrary/genetics/trisomy.html

  
 Chromosomal Abnormalities: Trisomy 18, Trisomy 13
Parents should be counseled on the very short expected lifespan of the newborn with trisomy 13 or 18.
This syndrome has an incidence of between 1 in 3000 and 1 in 8000, with a 3:1 F:M predominance.
Fuloria, M. The Newborn Examination I: Emergencies and Common Abnormalities Involving the Skin, Head, Neck, Chest, and Respiratory and Cardiovascular Systems.
http://pedclerk.bsd.uchicago.edu/chromosomalabnormalities.html

  
 What is Trisomy 13
Quite early on I think the doctors suspected what the problem was and started mentioning Trisomies and Syndromes.
Infants affected with Trisomy 13 tend to be small at birth.
Only a few may be present in any specific child.
http://www.babytoto.co.uk/T13.htm

  
 Population-Based Analyses of Mortality in Trisomy 13 and Trisomy 18 -- Rasmussen et al. 111 (4): 777 -- Pediatrics
trisomies or counsel families with infants or fetuses who have
For each condition, 91% of infants died within the first
we identified 70 liveborn infants with trisomy 13 and 114 liveborn
http://www.pediatrics.org/cgi/content/abstract/111/4/777

  
 TRISOMY 13
Baty, BJ, Jorde, LB, Blackburn, BL, Carey, JC (1994) Natural Histoy of Trisomy 18 and Trisomy 13:II Psychomotor Development.
Baty, BJ, Blackburn, BL, Carey, JC (1994) Natural History of Trisomy 18 and Trisomy 13:I Growth, Physical Assessment, Medical Histories, Survival and Recurrence Risk.
Trisomy 13 occurs with a frequency of about 1 in 9000 newborns.
http://www.cpdx.com/cpdx/trisom13.htm

  
 Trisomy 13 - AskTheBrain.com
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Trisomy 13 syndrome: Condition with three rather than the normal two chromosomes #13.
http://www.askthebrain.com/13_trisomy-.html

  
 Trisomy_13
Second-trimester maternal serum analyte levels associated with fetal trisomy 13.
Origin and mechanisms of non-disjunction in human autosomal trisomies.
Rates and survival of individuals with trisomy 13 and 18.
http://www.tdh.texas.gov/tbdmd/risk/risk10-trisomy13.htm

  
 Trisomy On-Line - Support for Families by Families
You may place your own candle if you wish.
Trisomy On-Line - Support for Families by Families
We are the current administrators of the Trisomy and the Rainbow Angel Wings Listservs respectively, on-line support groups for those whose lives have been touched by the diagnosis of a trisomy chromosomal disorder including Trisomy 18, Trisomy 13 and many other rarer Trisomy disorders.
http://www.trisomyonline.org/

  
 Mothers 35 Plus - the website for 'older mothers'. Down syndrome, trisomy 13 and trisomy 18
There are other Trisomy conditions in addition to the above, but these are not as common.
Read the story of Abigail, who had Trisomy 18.
Children born with Trisomy 18 suffer severe mental retardation, heart defects and other health problems.
http://www.mothers35plus.co.uk/questions.htm

  
 Rainbows Down Under - A Trisomy 18 & 13 Resource
What was available tended to be very medically orientated, negative and, as I found out, quite outdated.
Trisomy continues to distress me. These pages are my attempt to link others and help spread more accurate and up to date information about Trisomy and related disorders.
The main focus of this site is Trisomy 18, Trisomy 13 and other related chromosomal disorders.
http://members.optushome.com.au/karens

  
 Trisomy 13/18 / Family Village Library
SOFT has books for distribution including, "Trisomy 18 - A Book for Families," "Trisomy 13 - A Book for Families," and "Care of the Infant and Child with T-18 & T13." They collect information on physicians and researchers who treat/study the diseases and make that information available to members.
Hosts several on-line support groups for those whose lives have been touched by the diagnosis of a trisomy chromosomal disorder including Trisomy 18, Trisomy 13 and many other rarer Trisomy disorders.
This list is to bring parents, family, and friends of Trisomy 18 babies or children together.
http://www.familyvillage.wisc.edu/lib_tr38.htm

  
 trisomy 13 --  Encyclopædia Britannica
Overview of this British organization offering information and support for families affected by trisomy and related disorders.
Infants born with this disorder have profound mental retardation and severe developmental malformations that...
(E-trisomy, or trisomy 18), a congenital disorder associated with an additional 18th chromosome that occurs in 1 out of 3,000 live births.
http://www.britannica.com/eb/article?eu=2483&tocid=0

  
 Trisomy 13
There is so much need out there for decent resources.
There really isn't that much out there for Trisomy 13, so I'll keep looking and try to expand it.
Some people have come after querying for trisomy 13, and so I thought I would offer something for them.
http://www.tblog.com/templates/index.php?bid=wilsfordmindy&static=272597

  
 SCIENCE IMAGES-GENETIC-Trisomy 13
Like other trisomies, this disorder can arise from either nondysjunction or translocation.
Trisomy 13 - possibly first described by Bartholin in 1657, the syndrome occurs once in every 15,000 live births.
http://aci.mta.ca/Courses/Biology/Images/genetic%20folder/Trisomy13.html

  
 Trisomy 13 - DrGreene.com - caring for the next generation
Trisomy 13 was first described in 1657, but four hundred fifty years of medical knowledge have not improved the outlook for children born with this syndrome.
Trisomy 13 is often detectable on ultrasound as early as 10 weeks.
Even so, the risk of having another baby with trisomy 13 is usually very low, unless the trisomy 13 is a translocation.
http://www.drgreene.com/21_23.html

  
 Trisomy 13
The karyotype here demonstrates trisomy 13 (47, XX, +13) also known as Patau's syndrome.
This is a prominent bilateral cleft lip associated with trisomy 13.
Extra toes are seen here on each foot.
http://medgen.genetics.utah.edu/photographs/pages/trisomy_13.htm

  
 Trisomy On-Line - Message Boards
For example there is Tri-Med, for those who are pregnant and those who have an earthly angel with ANY trisomy disorder (full, partial, mosaic, tetrasomy, trisomy 1, trisomy 2, trisomy 3 etc etc).
There is also Tri-Choices, support specifically for those who have terminated or interrupted their pregnancy.
http://www.trisomyonline.org/messageboards.htm

  
 APP.COM - Charity founded in son's memory aids families
He was diagnosed with trisomy 13, also called Patau&, which causes congenital heart defects, brain development problems and breathing difficulties, which doctors discovered after a routine sonogram.
Michael Gerard Puharic was born on July 29, 2000.
http://www.app.com/app/story/0,21625,1031600,00.html

  
 SCIENCE IMAGES-GENETIC-Trisomy 13-15
Trisomy 13-15 - alternately known as Patau's syndrome, infants born with this condition are usually small for date, with typical facial appearance including a large broad nose, small eyes and a small mouth.
Meiotic non-dysjunction appears to be the cause of the extra chromosome in the 13-15 group.
http://aci.mta.ca/Courses/Biology/Images/genetic%20folder/Trisomy13-15.html

  
 Energy Citations Database (ECD) Document #133657 - Nondisjunction studies in trisomy 13
The origin of nondisjunction in trisomy 13 has previously been studied using cytogenetic heteromorphisms and RFLP markers, but it was not possible to determine the origin of the additional chromosome in all cases.
The addition of more DNA markers will enable the detection of the origin of nondisjunction in all cases and the study of altered recombination associated with nondisjunction, as previously described in trisomy 21 and 47,XXY.
Energy Citations Database (ECD) Document #133657 - Nondisjunction studies in trisomy 13
http://www.osti.gov/energycitations/product.biblio.jsp?osti_id=133657

  
 Late-Term Abortion Saved These Women's Lives
During a routine ultrasound (the only way to detect abnormalities that require late-term abortion), she discovered her baby had Trisomy 13, a chromosomal abnormality that causes severe deformities and carries no hope of survival.
Because her baby was already dying and because this put her own life at stake, Watts had an intact dilation and extraction (D and X), the procedure that Bush condemns as "brutal."
http://www.womensenews.com/article.cfm/dyn/aid/2046

  
 Michael Gerard Puharic Memorial Fund -trisomy 13 support, education and awareness
Michael Gerard Puharic Memorial Fund -trisomy 13 support, education and awareness
Michael’s Feat received the 2004 NMCC Crystal Beacon Award for Volunteer Organization of the Year
http://www.michaelsfeat.org/

  
 Unique - Rare Chromosome Disorder Support Group - www.RareChromo.org
The purpose of this web site is to describe the Unique Rare Chromosome Disorder Support Group and how to contact us.
Unique is a source of information, mutual support and self-help to families of children with any rare chromosome disorders including deletions, trisomy, balanced translocations, unbalanced translocations, rings, inversions, duplications, tetrasomy, monosomy, triploidy, isodicentric, marker, mosaic, sex chromosome aneuploidy (e.g.
Please find out more about Unique by browsing our website using the menu on the left.
http://www.rarechromo.org/

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