4 edition of Klinefelter Syndrome found in the catalog.
April 30, 2004
by Icon Health Publications
Written in English
|The Physical Object|
|Number of Pages||92|
What Is Klinefelter Syndrome? Klinefelter syndrome is a fairly common genetic condition found in males only.. Many boys with Klinefelter syndrome — also known as XXY syndrome — have no signs or symptoms, and some don't even know they have it until later in life.. The XXY condition that causes Klinefelter syndrome can't be changed, but medical treatment and working with therapists can help. Mary Quigg Genetics () W Maple Rd West Bloomfield, MI
Klinefelter syndrome (KS) was first described by Dr. Harry Klinefelter, an endocrinologist, in He identified a group of adults with infertility, hypogonadism, gynecomastia, and increased gonadotrophin levels (Klinefelter, Reifenstein, & Albright, ).In , these symptoms were linked to the extra X chromosome in these men (Jacobs & Strong, ). Klinefelter syndrome results when a boy is born with at least 1 extra X chromosome. This is written as XXY. Klinefelter syndrome occurs in about 1 out of to 1, baby boys. Women who get pregnant after age 35 are slightly more likely to have a boy with this syndrome than younger women. Symptoms.
Klinefelter syndrome is one of the most common chromosome conditions in newborns. It affects between 1 in and 1 in 1, newborn males. Author: Stephanie Watson. Among the treatments for Klinefelter syndrome include therapy that replaces testosterone hormone and surgery that reduces breasts. If necessary, physical, language, occupational and speech therapy can also be used. Order an essay on Klinefelter’s syndrome online. Klinefelter’s syndrome is a chromosomal disorder that affects males.
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The KS Story is the culmination of twelve years ongoing study and an emotional journey through the workings of the congenital chromosome condition Klinefelter’s Syndrome (KS).
The book was created primarily as a conduit to respected support groups, medical specialists and research units, with a chapter devoted to further study, including a comprehensive support address and online section and a selection of books.
I bought this book hoping to find some current information on Klinefelters Syndrome as the book is titled a Source Book BUT here is where my understanding was incorrect. The book contains about 50% detail on how to look up Medical Journals to do your own research.2/5(1).
Living with Klinefelter Syndrome, Trisomy X, XYY: A guide for families and individuals affected by X and Y chromosome variations by Virginia Isaacs Cover MSW |.
Klinefelter's syndrome Klinefelter’s syndrome (KS) was ﬁrst described by Harry Klinefelter in as an endocrine disorder of unknown etiology.
InJacobs et al recognized KS as a chromosomal disorder in which the patients had an extra X chromosome to a normal male karyotype, 46 XY (1). Understanding Klinefelter Syndrome, A Guide for XXY Males and Their Families, by Robert Bock (), National Institute of Health; Available free of charge by calling Klinefelter Syndrome, For Boys Only, A Supplement, by Diane Plumridge, Christine Barkost, and Stephen La Franchi ():Oregon Health Sciences Center.
Klinefelter syndrome is a chromosomal condition in boys and men that can affect physical and intellectual development. Most commonly, affected individuals are taller than average are unable to father biological children (infertile); however the signs and symptoms of Klinefelter syndrome vary among boys and men with this condition.
Kleinfelter syndrome facts author: John P. Cunha, DO, FACOEP. Klinefelter syndrome, also known as the XXY condition, is a term used to describe males who have an extra X chromosome in most of their cells. About one of every males has an extra X chromosome, but many don't have any symptoms.
Because symptoms of Klinefelter syndrome (KS) can sometimes be very mild, many people are never diagnosed or treated. When a diagnosis is made, treatment is based on the signs and symptoms present in each person, especially the problems related to hypogonadism, gynecomastia, and psychosocial problems.
Treatment may include: Testosterone replacement: About half of people with. Definition of Klinefelter's Syndrome Klinefelter's syndrome is the most common sex chromosome disorder and results in primary hypogonadism and infertility in men.
The syndrome is caused by an additional X chromosomes resulting in a karyotype of 47, XXY. Synonyms: XXY syndrome, 47. Try the new Google Books. Check out the new look and enjoy easier access to your favorite features Heidelberg hormone human hypogonadal increased karyotype Kline Klinefelter boys Klinefelter patients Klinefelter syndrome Klinefelter's syn Klinefelter's syndrome Lancet leg ulcers Leydig cells mean meiotic mental mosaic Munchen nefelter 5/5(1).
Klinefelter syndrome is one of the genetic disorders in males. It occurs when a male baby is born with more than required or extra X chromosomes. Many males consist of one X and one Y chromosome and an extra chromosome can cost a male with physical traits which are inappropriate for males.
Klinefelter syndrome is associated with an increased risk for breast cancer, a rare tumor called extragonadal germ cell tumor, lung disease, varicose veins and osteoporosis. Men who have Klinefelter syndrome also have an increased risk for autoimmune disorders such as lupus, rheumatoid arthritis and Sjogren's syndrome.
Klinefelter syndrome (KS) is a condition that occurs in males when they have an extra X males with KS have no obvious signs or symptoms while others may have varying degrees of cognitive, social, behavioral, and learning difficulties.
Klinefelter syndrome is a group of conditions affecting the health of males who are born with at least one extra X chromosome.
Klinefelter Syndrome (47, XXY) is a chromosomal variation in males in which one extra X chromosome is present, resulting in a XXY sex chromosome karyotype. The extra X chromosome can affect physical, developmental, behavioral, and cognitive functioning.
Klinefelter Syndrome is an inherited disorder of the sex chromosome in which an extra X chromosome is present (XXY) Klinefelter syndrome is a genetic disorder that happens in males with an extra X chromosome. It happens in males and is linked with hypo-gonads and infertility.
Klinefelter syndrome happens in about 1 out of to 1, baby boys. Klinefelter syndrome is caused by an additional X chromosome. This chromosome carries extra copies of genes, which interfere with the development of the testicles and mean they produce less testosterone (male sex hormone) than usual.
Klinefelter syndrome gets its name from a publication in by Klinefelter, Reifenstein, and Albright describing a series of patients with gynecomastia, small testes, aspermatogenesis, androgen deficiency, and increased levels of follicle stimulating hormone.
Of particular interest at that time was the association of primary hypogonadism with high levels of gonadotrophins. Characteristic clinical findings in men with Klinefelter syn-drome. Note that there are no facial characteristics that suggest a Abramsky L, Chapple J. 47,XXY (Klinefelter syndrome) XYY File Size: KB.
Klinefelter syndrXXY was first described 70 years ago ().With an incidence of % to % of male neonates (i.e. 1 to 2 per ), it is one of the commonest congenital chromosome disorders resulting in hypogonadism and genetically-determined infertility (2, 3).Klinefelter syndrome is associated with a significantly higher morbidity rate compared to the male population as a by:.
The account given by Klinefelter came to be known as Klinefelter syndrome as his name appeared first on the published paper, and seminiferous tubule dysgenesis was no longer used. Considering the names of all three researchers, it is sometimes also called Klinefelter–Reifenstein–Albright ciation: /ˈklaɪnfɛltər/.An extra or missing sex chromosome yields a syndrome called sex chromosome aneuploidy.
A syndrome is a collection of symptoms and physical signs. In some females, the manifestations of 47,XXX, are mild and barely noticeable while in others, there are much more severe symptoms.
My baby may have Klinefelter’s syndrome, but it doesn’t define who he is. I know there will be lots of obstacles along our Klinefelter syndrome journey, but we are prepared to do whatever it takes to make sure Chase is happy and healthy!