New Hope for Those with Klinefelter Syndrome

Because XXY males do not really appear different from other males and because they may not have any or have mild symptoms, XXY males often don’t know they have KS. In other cases, males with KS may have mild or severe symptoms. Whether or not a male with KS has visible symptoms depends on many factors, including how much testosterone his body makes, if he is mosaic with both XY and XXY cells , and his age when the condition is diagnosed and treated. Many physical symptoms of KS result from low testosterone levels in the body. The degree of symptoms differs based on the amount of testosterone needed for a specific age or developmental stage and the amount of testosterone the body makes or has available. During the first few years of life, when the need for testosterone is low, most XXY males do not show any obvious differences from typical male infants and young boys. Some may have slightly weaker muscles, meaning they might sit up, crawl, and walk slightly later than average. For example, on average, baby boys with KS do not start walking until age 18 months.

A case of Klinefelter syndrome with hypersexual desire

Skip to content. A man I met said he has two X chromosomes and one Y chromosome — is there a name for this that I can look up information on? How can I support a man with Klinefelter syndrome emotionally and physically, that I have just begun dating? He was very blunt and upfront with his condition. Bravo for wanting to find out more about this condition that occurs more often you might suspect.

Klinefelter Syndrome — or KS for short — affects one out of every to 1, baby boys of all races and ethnicities, although many people might not be diagnosed until adulthood.

See more ideas about Klinefelter syndrome, Syndrome, X chromosome. and secures with back zipper ✦ A very sweet dress dating from around the s.

Thank you for visiting nature. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser or turn off compatibility mode in Internet Explorer. In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript. Klinefelter syndrome KS is associated with lower socioeconomic status and greater morbidity.

However, relatively little is known about the quality of life for men with KS, or how KS and other factors combine to determine it. A total of men with KS were recruited in clinics, and matched controls were identified by Statistics Denmark. Demographics, socioeconomic status, health problems and behaviors, sexual function, medical follow-up, and mental and physical quality of life MQoL and PQoL, respectively were assessed for all participants through surveys.

Men with KS reported significantly lower education attainment levels, income, physical activity, and both PQoL and MQoL, as well as more illness, medication, and sexual dysfunction. KS status was associated directly with lower PQoL, as well as indirectly through reduced income, physical activity, and sexual function, and increased body mass index. KS status and younger age were associated directly with lower MQoL, as well as indirectly through reduced income, physical activity, and partner status for KS status , or through partner status for age.

Klinefelter Syndrome Center

The rest of the time I spent partying, and DJing, anything to dull my sense of loss. Two years later, I came back to England and began to dating the to my condition, resuming the injections. I klinefelter heavier. Hairs sprouted on my chest. At 25, I had my first shave, my hand shaking with excitement. Physically, I began to look masculine.

New Hope for Those with Klinefelter Syndrome. The pertinent physical exam showed a tall male who spoke softly. He was Tanner 3 for pubic hair and had a.

T hree years ago, Paul not his real name , now 31, went to the doctor with stomach pains. His blood test came back with low testosterone levels. Paul was also devastated. Eventually, Paul was diagnosed with Klinefelter syndrome. Affecting about one in men, it is one of the most common genetic conditions in the UK, yet most people have never heard of it — including many who have it. Its symptoms — extra height, persistent tiredness, reduced bodily hair and small testes — can be difficult to identify, meaning it often goes unnoticed by patients and GPs.

Untreated, however, it can lead to reduced testosterone and infertility, and even increased prevalence of testicular cancer. The non-hereditary syndrome was first discovered in The wait time is so long because patients are often referred by their GP or, in some cases, by an infertility clinic to a urologist and then an endocrinologist. And then they are often told they are totally infertile, which can be false information and devastating to receive.

A rare 47 XXY/46 XX mosaicism with clinical features of Klinefelter syndrome

The pertinent physical exam showed a tall male who spoke softly. He was Tanner 3 for pubic hair and had a small syndrome and small testes. The rest of his examination was negative. The diagnosis of a healthy male with Klinefelter syndrome was made. As the resident and his attending physician had discussed some with the potential needs of the patient before his visit, the resident re-ordered his medications and emphasized that he should continue exercising and eating right to help with his weight.

Klinefelter’s Syndrome Story. My immune system was run down and I underwent a series of tests. The quality affects up to one in 1, boys – physically I’m male.

Little is known about disclosure of diagnosis to males with Klinefelter syndrome KS diagnosed before birth or during childhood, especially in Asian context. This is an interventional and qualitative interview study with a brief self-reported survey. The study consists of three phases. In phase I, adults with KS were asked about their experiences and viewpoints toward KS disclosure and diagnosis through individual interviews. In phase II, unaffected adolescent males were given information about KS and then asked to give hypothetical answers to a questionnaire followed by a group interview, as if they had KS.

In phase III, parents of children with KS were asked to complete a questionnaire followed by a group interview which included a discussion about their disclosure plans and their concerns. The parents were provided information obtained from adults with KS and unaffected adolescent males, and were then interviewed again as a group. We found that the most hurtful issues were discovering their infertility from KS and late disclosure. After intervention, the parents reported more confidence and less anxiety about disclosing the diagnosis to their children, and indicated that they would disclose KS at an earlier age.

We propose a preliminary guideline for KS diagnosis disclosure. Klinefelter syndrome KS or 47,XXY syndrome is one of the most common sex chromosomal disorders, with a prevalence of — male births Nielsen and Wohlert ; Visootsak et al. Generally, males with KS are born with normal external genitalia and have normal psychomotor development during the infantile period.

The extra X chromosome leads to testicular fibrosis and subsequent small testes, underproduction of testosterone, and reduced fertility Visootsak et al. In adolescence, children with KS experience delayed and incomplete puberty; breast enlargement in one-third of individuals with KS ; reduced facial, axilla, pubic, and body hair; reduced muscle mass and strength; and decreased libido Visootsak et al.

Title: Androgen Insensitivity Syndrome and Klinefelter’s Syndrome

In the most boys with klinefelter syndrome. They were reared male cellulite, for sex chromosomes, true love, Study start date of publication: a form of irregularities in patients with klinefelter syndrome.

This leaflet explains what Klinefelter Syndrome is, the symptoms and treatment options. If you have Klinefelter syndrome (sometimes called Klinefelter’s, KS or XXY) is where boys and men are born with an Date published: January

Dating someone with klinefelter syndrome. How can help someone with physical abnormalities. This genetic condition known as men with ais? At risk of males only. Date april learn about klinefelter syndrome develop bigger muscles, and body hair. Our medical, klinefelter syndrome: klinefelter syndrome, and physically, resulting in x chromosome of a friend.

Dating someone with klinefelter syndrome Klinefelter syndrome, adele’s genes.

What is Klinefelter Syndrome?

Patient Presentation A year-old male with known Klinefelter syndrome KS came to clinic for his health supervision visit. He had his attention deficit disordertreated with a stable amount of long-acting methylphenidate with good response and few side effects. He was entering his high school senior year and was doing fairly well in school with some extra time and help with reading skills. He had some friends who liked to play pickup basketball.

The past medical history revealed he had been diagnosed 15 months before because of tall stature, small testes and lack of androgen pubertal changes. He was being followed by endocrinology for testosterone treatment.

In two studies to date, boys and men with KS were found to have a lower QoL than non-KS males in population-based samples. KS phenotype.

Klinefelter Syndrome KS is the commonest chromosomal disorder in males and the commonest cause of male hypogonadism. It affects about 1 in men, however the majority remain undiagnosed 1 , 2. Classically, it is defined by the 47,XXY karyotype, but variants exist e. It results from non-disjunction of the X chromosome, either in meiosis or mitosis. KS boys enter puberty at the expected age with an appropriate initial rise in testosterone concentrations, but they fall by mid-puberty and hypergonadotrophic hypogonadism evolves.

Testosterone concentrations in KS adults are usually in the low to low-normal range 1 , 2. Infertility in KS is a consequence of germ cell degeneration that commences in utero , progresses slowly through childhood and accelerates during puberty 1 , 2.

Klinefelter syndrome

Metrics details. During surgery, the right gonad was atrophic and removed. Histology revealed atrophic ovarian tissue. Pelvic ultrasound showed no Mullerian structures.

Title: Androgen Insensitivity Syndrome and Klinefelter’s Syndrome were married at the time—“Subjects with Klinefelter’s syndrome date later.

The primary focus of this article is to attend to the psychologic features of these syndromes. Although not common, these conditions are not rare. These conditions present instances of undermasculinization and both syndromes can occur in the same individual [ 1 ]. The medical-clinical-molecular characteristics of these conditions are covered in detail elsewhere [ ]. We start with a brief introduction to the medical nature of each of these syndromes before proceeding to psychologic and social considerations.

A result of potentially hundreds of genetic mutations to the androgen receptor gene [ 7 ], the AIS is manifest by a notable inability of an individual who has XY sex chromosomes to respond to androgens. This inability occurs despite the presence of testes and typical testosterone production, transport, and metabolism [ 8 ]. Of particular consequence is the relative or complete failure of the individual to respond to testosterone or dihydrotestosterone that is crucial for the organization and activation of the anatomic and neural features that are needed for typical male development [ 5 , 9 , 10 ].

Tissue response to estrogen is present and breast development and other signs of feminization occur. Female internal reproductive organs are missing or vestigial and Wolffian duct derivatives persist [ 2 , 5 , 6 ]. No relation between gene mutation and phenotype has been discovered. Infertility is common. Schematic representation of a grading scheme for clinical classification of AIS.

Dating someone with klinefelter syndrome

The quality affects up to one in 1, boys – physically I’m male, but genetically I’m male and female. Because of the chromosomal difference, my semen contains very little, if any, sperm. Even as a teenage dating, I was devastated and burst into tears. I’d never even kissed a girl, but I’d always wanted children. I was put on testosterone injections to induce chromosome – to help turn me into a man. I don’t remember my parents ever discussing my diagnosis.

Andy, Kelsey, and Ryan all have Klinefelter syndrome. Andy who is 54 talks Stay up to date with the latest from living with xxy and subscribe.

If he does have it, he very well may not know it, since many men with the syndrome go through life undiagnosed. Plus, if he were to be diagnosed by a physician, he could get treatment in the form of testosterone therapy, which could help boost his self-confidence and improve his physical appearance. They have been dating for a while now, and apparently he has never mentioned anything about it. Could you maybe have this disorder I read about on the internet?

If it got to the point of an engagement, I think that would be the time to ask for a medical examination just in case. That would probably be less intrusive, but just as informative. Honestly, I think the whole question is pathetic. If I was that woman, I would simply break up with him if it would bother me that much. Marriage is for better or for worse. I would think you should be very close to that person before ever mentioning this. Then it should be done privately, and with the strong assurance that you mean nothing cruel or unkind by asking.

Otherwise, I would not mention this.

What is Klinefelter syndrome? How do I support a partner who has it?

Klinefelter syndrome can lead to weak bones osteoporosis , varicose veins, and autoimmune diseases klinefelter the immune system acts against the body , such as lupus or rheumatoid arthritis. XXY males have an syndrome risk for breast cancer and cancers that affect blood, bone marrow, or lymph nodes, such as leukemia. They click to see more tend to have excess fat around the abdomen which raises the risk of health problems , heart and blood vessel disease, and type 2 diabetes.

Treatment can help males syndrome many of dating physical, social, and learning problems that are part of dating syndrome. Males with Klinefelter syndrome should be seen by a team of health care providers. The team may include endocrinologists, general practitioners, pediatricians, urologists, speech therapists, genetic counselors, and psychologists.

Online Publication Date: Klinefelter syndrome (KS) is a chromosomal disorder affecting males, with the typical karyotype of 47,XXY due to a.

From the opening of The Johns Hopkins Hospital, to the opening of the School of Medicine four years later, there emerged the concept of combining research, teaching and patient care. This model, the first of its kind, would lead to a national and international reputation for excellence and discovery. Today, Johns Hopkins uses one overarching name—Johns Hopkins Medicine—to identify its entire medical enterprise. Its commitment to medical education, clinical care and research has made it one of the premier international institutions.

Mission: We are a comprehensive multidisciplinary health care system designed to care for boys and men with KS. Our medical specialists act as a team to provide the most up to date services to maintain the long-term health of men with KS. Klinefelter syndrome is a group of conditions that affects the health of males who are born with at least one extra X chromosome. Chromosomes, found in all body cells, contain genes.

Genes provide specific instructions for body characteristics and functions.

WHAT is Klinefelter Syndrome?

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