Klinefelter Syndrome Causes, Karyotype, Diagnosis, Treatment
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.
Sindrom Klinefelter, Penyakit yang Disebabkan oleh Kondisi
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.
Study Pustaka Sindrom Klinefelter PDF
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.
Klinefelters Syndrome Article Presentation
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.
O Que é Síndrome De Klinefelter
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.
Cos'è la sindrome di Klinefelter? • +Plus! Magazine
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.
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.
Sindrom Klinefelter.ppt
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.
Makalah Sindrom Klinefelter PDF
Anak laki-laki remaja dengan sindrom Klinefelter mungkin memiliki beberapa atau semua tanda fisik di bawah ini. Tubuh lebih tinggi dari rata-rata. Kaki lebih panjang. Badan lebih pendek. Pinggul lebih besar dibanding anak lain. Anak laki-laki terlambat mengalami pubertas. Massa otot dan rambut lebih sedikit.
Klinefelter Syndrome Causes, Karyotype, Diagnosis, Treatment
Klinefelter Syndrome. Klinefelter syndrome is a common genetic condition in which people assigned male at birth (AMAB) have an additional X chromosome. Symptoms may include breast growth, infertility, osteoporosis and learning difficulties. Treatments usually involve physical and emotional therapy, as well as hormone replacement.
Sindrom Klinefelter gejala, diagnosis, rawatan
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.
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 PDF
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.
Makalah Sindrom Klinefelter dan Sindrom Down TUGAS MAKALAH SINDROM
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 Merupakan Suatu Kelainan Kromosom PDF
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.
Makalah Askep Sindrom Klinefelter PDF
Introduction. Klinefelter syndrome (KS) is a common male chromosomal disorder (47, XXY) that has been a topic of intrigue and inquiry since the 1940s, when it was first described 1. It is a subject of interest because of its wide spectrum of clinical manifestations, which include certain physical features, cognitive delays, and azoospermia.
