Makalah Sindrom Klinefelter PDF
Klinefelter syndrome is a genetic condition affecting males, and it often isn't diagnosed until adulthood. Klinefelter syndrome may adversely affect testicular growth, resulting in smaller than normal testicles, which can lead to lower production of testosterone. The syndrome may also cause reduced muscle mass, reduced body and facial hair, and.
Sindrom Klinefelter
Abstract. Sindrom Klinefelter (SK) merupakan kelainan akibat adanya kromosom seks tambahan (47,XXY) yang menyebabkan hipergonadotropik hipogonadisme, dan infertilitas. Penampilan pasien SK hampir.
Makalah Askep Sindrom Klinefelter PDF
Gejala Sindrom Klinefelter. Seseorang dengan sindrom ini cenderung memiliki testis yang kecil, sehingga tidak dapat menghasilkan testosteron pada kadar normal. Testosteron memiliki peran penting dalam tahap pubertas seorang laki-laki, sehingga kekurangan testosteron menyebabkan proses pubertas yang terhambat atau bahkan tidak komplet.
(DOCX) Makalah Askep Sindrom Klinefelter DOKUMEN.TIPS
Gejala Sindrom Klinefelter dan Ciri-cirinya. Pengidap sindrom klinefelter memiliki jumlah sperma yang lebih sedikit. Akibatnya, mereka cenderung kesulitan untuk memiliki keturunan. Namun, kemungkinan itu masih ada. Pengidap sindrom klinefelter masih bisa memiliki keturunan dengan menjalani terapi ke dokter kandungan atau profesional medis lainnya.
Sindrom Klinefelter gejala, diagnosis, rawatan
Treatment. If you or your son is diagnosed with Klinefelter syndrome, your health care team may include a doctor who specializes in diagnosing and treating disorders involving the body's glands and hormones (endocrinologist), a speech therapist, a pediatrician, a physical therapist, a genetic counselor, a reproductive medicine or infertility specialist, and a counselor or psychologist.
Sindrom Klinefelter Merupakan Suatu Kelainan Kromosom PDF
Klinefelter syndrome occurs when a male is born with an extra X chromosome. Thus a male with Klinefelter has XXY instead of the usual XY pair. Because males with this condition produce less of the male hormone testosterone than other males, they are less masculine-looking than their peers. The condition usually leads to infertility in adult.
Study Pustaka Sindrom Klinefelter PDF
Kurangnya kadar testosteron di dalam tubuh akibat sindrom Klinefelter dapat meningkatkan risiko terjadinya beberapa penyakit berikut: Gangguan mental, seperti cemas atau depresi. Gangguan emosi atau perilaku, seperti merasa rendah diri atau berperilaku impulsif. Mandul ( infertilitas) Disfungsi seksual.
Sindrom Klinefelter Dan Penatalaksanaannya Blok27 David PDF
Clinical phenotype. The major signs and symptoms of Klinefelter Syndrome (KS) have been well characterized since the first description of the disease [].As traditionally described, patients with KS have tall stature, small testes, gynecomastia in late puberty, gynoid aspect of hips (broad hips), sparse body hair, signs of androgen deficiency and low serum testosterone coupled with elevated.
Makalah Sindrom Klinefelter dan Sindrom Down TUGAS MAKALAH SINDROM
Klinefelter syndrome (KS) is the most common sex chromosomal abnormality affecting approximately 1 in 500-700 males. It is usually associated with the occurrence of an extra X chromosome [].In addition, it is an endocrine disorder associated with tall stature, gynaecomastia, hypogonadism, small testes, impaired spermatogenesis and androgen deficiency.
Cos'è la sindrome di Klinefelter? • +Plus! Magazine
Klinefelter's syndrome. Klinefelter's syndrome is the most common cause of testicular failure that results in impairments in both spermatogenesis and—to a lesser extent—testosterone production. This syndrome is the most common sexchromosome disorder affecting 1 in 500 men across all ethnic groups, but the diagnosis is often delayed because.
Makalah Askep Sindrom Klinefelter PDF
Abstract. Although Klinefelter syndrome (KS) is common, it is rarely recognised in childhood, sometimes being identified with speech or developmental delay or incidental antenatal diagnosis. The only regular feature is testicular dysfunction. The postnatal gonadotropin surge (mini-puberty) may be lower but treatment with testosterone needs.
Sindrom Klinefelter.ppt
Klinefelter syndrome (KS), caused by the presence of an extra X chromosome, is the most prevalent chromosomal sexual anomaly, with an estimated incidence of 1:500/1000 per male live birth (karyotype 47,XXY). High stature, tiny testicles, small penis, gynecomastia, feminine body proportions and hair, visceral obesity, and testicular failure are all symptoms of KS.
O Que é Síndrome De Klinefelter
Abstract. Sindrom Klinefelter (SK) merupakan kelainan akibat adanya kromosom seks tambahan (47,XXY) yang menyebabkan hipergonadotropik hipogonadisme, dan infertilitas. Penampilan pasien SK hampir tidak berbeda dengan mereka yang berkariotip normal, tanpa gejala klinis yang khas selama masa anak, sehingga diagnosis ditegakkan setelah usia remaja.
Klinefelter Syndrome Causes, Karyotype, Diagnosis, Treatment
Sari. Sindrom Klinefelter (SK) merupakan kelainan akibat adanya kromosom seks tambahan (47,XXY) yang menyebabkan hipergonadotropik hipogonadisme, dan infertilitas. Penampilan pasien SK hampir tidak berbeda dengan mereka yang berkariotip normal, tanpa gejala klinis yang khas selama masa anak, sehingga diagnosis ditegakkan setelah usia remaja.
Sindrom Klinefelter PDF
Klinefelter syndrome is a sex chromosome disorder in individuals who were assigned male at birth that results from the presence of an extra X chromosome in cells. People typically have 46 chromosomes in each cell, two of which are the sex chromosomes. Females typically have two X chromosomes (46,XX), and males typically have one X and one Y chromosome (46,XY).
SINDROM KLINEFELTER ??!! Kenali Penyebab, Gejala, Dan Penanganan
Klinefelter syndrome (KS) results from 2 or more X chromosomes in a phenotypic male. The clinical phenotype of KS was first described by American physician Dr. Harry Klinefelter in 1942.[1] The syndrome describes males with tall stature, small testes, gynecomastia, and azoospermia. The precise genetic etiology of supernumerary X chromosomes (47,XXY) was identified in 1959.[1][2] Extra X.