Even doctors, no less, made wise-ass cracks at me. The main cause for Turner’s syndrome is still being studied, but some theories support its development. Turner Syndrome – Life expectancy Women living with Turner syndrome live up to fifty years. For girls and women who are treated promptly and follow their treatment plans, they can have a normal or near-normal life expectancy. We divorced in l989. Hang in there girls! Im married 7 yrs and just finished a failed attempt at ivf . I was kept in the nicu for weeks. Females have two X chromosomes (XX) while males have one X and one Y chromosome (XY). She was diagnosed before birth. I accept this missive sounds selfish with “poor me” thrown in for good measure but that is not what I wish to portray. Turner’s syndrome is commonly called Bonnevie-Ullrich-Turner syndrome or Ullrich-Turner syndrome in Europe because early doctors there also described the disease. These chromosomes contain the genes and DNA responsible for building the body. See answer, How can I learn more about learning disabilities in women and girls with Turner syndrome? We tried several cycles of IVF to no avail and whilst all the parameters looked ok eg womb thickness, E & P hormones levels it wasn’t working. Now I am only 4’7” but I’m ok with that which is why I chose not to do the shots. I would like to know everything you care to tell me about growth hormone shots. It is often corrected by supportive treatments such as egg donation from normal women. I have had some hard times, it’s understandable that you are scared. Life expectancy reduces by around thirteen years. According to SyndromesPedia, those with Turner's syndrome have a typical reduction of life expectancy of 13 years. I had perfect health until I contracted Lyme disease, and even with that, I continue to lead a normal life. 2. I was made fun of as a teenager for being small, but I never let it bother me. I had a great childhood and teenage life. Alot of these posts are old but its good to read different stories about ts . She had blood tests done and that was when we found out she had TS. The whole time the doctors told my parents I wouldn’t live to be two weeks old. This Doesnt mean that u will have answers right away as for why. Diabetes, high blood pressure, Addison disease, Cpap, and high chloresterol. Get the latest public health information from CDC: https://www.coronavirus.gov (link is external) However, girls and women with Turner syndrome are … In general, Turner Syndrome women are big readers, though we have trouble with math. If you get involved with someone who wants kids but isn’t patient or supportive enough to work with you to have them, then they are probably with the wrong person for you. I am now on ozempic and am losing weight. Do any of the members participating on this forum happen to have any knowledge about turner syndrome? To determine the exact genetic problem in an individual female, karyotyping is done. She has had issues with ear infections and multiple sets of tubes. Can you explain to us about the testing she is about to go thru, hi everyone my name is megan I have a lil girl with ts her name Is zoey she will be 2 in july… she is very out going she loves to play with kids my ? I’ll pray for your family! Sex hormones are usually given to improve sexual development. She loved to sing & had a beautiful voice. Once these were fixed she got pregnant immediately after the next two frozen embryo transfers. Women with this condition tend to be shorter than average and are usually unable to conceive a child because of an absence of ovarian function.Other features of this condition that can vary among women who have Turner syndrome include: extra skin on the neck (webbed neck), puffiness or swelling of the hands … I have a little sister with Turners. My newborn granddaughter was diagnosed with TS after they discovered she had coarctation of the aorta. She has always had a normal checkup, although if I remember correctly, they can develop a thinning of the aorta at a later time especially if they are on growth hormones. And giving person you will ever meet I am 5 feet 2 inches tall. During conception, the sex chromosomes are not transferred properly leading to the condition. I wish I would have found this site a long time ago. I have a bicuspid aortic valve, but no narrowing of the aortic arch. I get ocd and bet I have cried over this site many times ..so good to hear from healthy happy ts women ..and syndromes Pedia and all these other sites need to update..hurts me, I am a 23 yr old wife of five yrs…my husband and I lost our daughter in june 2011 to turner syndrome…difficult thing to experience…. Its like women and men aren’t fascinated except it¡¯s something to do with Woman gaga! I also tell my children everyone has something, either it is on the inside or the outside but everyone has something. The treatment for Turner’s Syndrome relies on improving the growth and sexual functioning of the woman. I am 56 years old. You can help advance My wife has TS and I remember when she told me she was so shamed that she couldn’t have children. She was a gymnast in grade school and high school. She was talking by walking by a year,, and is very smart! She married a nice guy but we think that after 15 years of him not helping and not wanting to adopt —- I think she just couldn’t take it anymore. When Turner’s Syndrome is detected before delivery, parents undergo genetic counseling to help them cope with the condition. is does ts effect your walking ? The short stature of course had been an issue of making fun of her plus she even had a music instructor not allowing her to be a drum major because she was too short. my 10 year old just got diagnosed…heart tests came out fine, small cyst in 1 kidney and ovaries of course underdeveloped…my question is the heart issue…we were told by 3 different doctors that once you check the heart and valves and its normal there would be no reason to check it again…yet i read here that some check every couple of years…anybody really know the answer,,,btw she has mosaic TS..starting hgh this week…thanks. I spent the next year recovering in hospital, learning to walk, talk and do all the basics again as well as bringing up my new twin babies with my husband. This section provides resources to help you learn about medical research and ways to get involved. Aside from sexual dysfunction, individuals with Turner’s syndrome have cognitive limitations specifically in memory, mathematical and spatial skills. My only symptoms were shortness of stature and lack of puberty. My Baby Has Turner Syndrome Congratulations! One bust. Sadly, my sister committed suicide 2 weeks ago. Physicians also assist the woman with certain reproduction techniques to help her become pregnant such as the use of donor eggs. Hi My name is Julie, I am 57 years old & was diagnosed with Turner’s Syndrome when I was 15 years old. Health wise im perfect . Hello. (And thus far – no cardiac surgeries!) Thanks, my ob/gyn explained to me a few things about that. These hormones are usually affected by the change in estrogen levels. Females with Turner’s Syndrome usually reach 50 years of age. I absolutely love this site. Since the condition is associated with chromosomal aberrations, there is no current cure to completely eradicate the condition. It’s Mary again. We weren’t serious then but I took her to an IVF centre as I felt for her and believed this new treatment option could help her. The most common congenital heart anomalies include post-ductal coarctation of the aorta, bicuspid aortic valve, partial anomalous venous drainage, aortic valve stenosis, aortic dissection, dilatation and rupture and hypoplastic left heart syndrome. How do I cope with this disease? You’re so intelligent. I have a pacemaker. My advice is that when you are ready to have children is to use the natural hormones to create a menstrual cycle and get a full blood test to check if any other hormone levels are out of wack. As with the other posts on this site, my daughter is great. Although historically, conjugated equine estrogens (CEE) such as Premarin® had been the preferred method of estrogen replacement in Turner… Turner syndrome is related to the X chromosome, which is one of the two sex chromosomes.People typically have two sex chromosomes in each cell: females have two X chromosomes, while males have one X chromosome and one Y chromosome.Turner syndrome results when one normal X chromosome is present in a female's cells and the other sex chromosome is missing or structurally altered. 23rd chromosome missing in Turners syndrome, Picture 2 – Symptoms and signs of Turners syndrome, Picture 3 – broad shield chest in Turner’s syndrome, Picture 4 – Puffy Feet in Turners syndrome, Image Source – Turnersyndromepictures.com. I was not diagnosed until age 22 or 23. I recently had a hysterectomy. Also, I was wondering if women with Turner syndrome are able to have a normal sexual life or if it is harder for them to get sexually aroused because of hormone differences. This means she may have one X-chromosome, two complete X-chromosomes, or one norm… Kerry’s womb was apparently the smallest (~2 cm) they had a pregnancy in at that time but it worked. 1998; 51:147–158. As she is 18 Doctor will not talk to me without hr being in the room.she plays harp. But many are, and what others need to know is that is o.k….so it won’t be exactly what you thought it would be like….it could be better! They are both the coolest two people I know. A normal female has 46 chromosomes, including 2 X-chromosomes (44XX). My sistercwas diagnosed with Turner’s around 5 years old. I have had a normal life and really enjoy my family. She made so many friends and they are so much alike. She was a straight A student and a honor student. Just keep Faith & Trust in God! 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