نتایج جستجو برای: klinefelter

تعداد نتایج: 1325  

Small supernumerary marker chromosomes (sSMCs), or markers, are abnormal chromosomal fragments that can be hereditary or de novo. Despite the importance of sSMCs diagnosis, de novo sSMCs are rarely detected during the prenatal diagnosis process. Usually, prenatally diagnosed de novo sSMCs cannot be correlated with a particular phenotype without knowing their chromosomal origin and content; ther...

Journal: :Orphanet Journal of Rare Diseases 2006
Jeannie Visootsak John M Graham

The term Klinefelter syndrome (KS) describes a group of chromosomal disorder in which there is at least one extra X chromosome to a normal male karyotype, 46,XY. XXY aneuploidy is the most common disorder of sex chromosomes in humans, with prevalence of one in 500 males. Other sex chromosomal aneuploidies have also been described, although they are much less frequent, with 48,XXYY and 48,XXXY b...

Journal: :Neurologia medico-chirurgica 2009
Takashi Sasayama Katsu Mizukawa Yoshio Sakagami Takashi Mizowaki Kazuhiro Tanaka Chiho Ohbayashi Kiyoshi Mori Sohei Kitazawa Eiji Kohmura

A 54-year-old man with Klinefelter syndrome presented with glioblastoma multiforme manifesting as a 2-week history of motor weakness of the bilateral extremities. Magnetic resonance imaging showed multiple heterogeneously enhanced tumors in the bilateral frontal lobes. Angiography showed no tumor stain or arteriovenous shunt. The tumor was partially removed through a right craniotomy. The histo...

2016
Hongjuan Fang Jian Xu Huanwen Wu Hong Fan Liyong Zhong

Klinefelter syndrome (KS) is the most common chromosomal aneuploidy in male population, which demonstrates an unusual association with acromegaly. We herein present a rare case involving the confirmation of KS 2 years after surgical treatment for acromegaly.A 27-year-old man presented with an acromegalic appearance. Endocrinological examination revealed a high growth hormone (GH) concentration,...

Journal: :The Japanese Journal of Urology 1989

Journal: :Revista Portuguesa de Endocrinologia, Diabetes e Metabolismo 2021

2004
Daniel H. Geschwind Elisabeth Dykens

Klinefelter Syndrome (KS) is a relatively common (1/500 to 1/1,000) genetic syndrome caused by an extra X chromosome in males, leading to an XXY karyotype. In most cases, the physical and neurobehavioral characteristics of KS are relatively mild, and KS is not usually associated with moderate or severe mental retardation. However, KS is often associated with significant language-based learning ...

Journal: :Journal of medical genetics 1971
H S Chandra G N Reddy J Peter G Venkatachalaiah

Case Report The patient was first seen by one of us (G.N.R.) when he was in St Martha's Hospital being treated for viral hepatitis. He is a dull-looking boy with a rather large build for his age. The lower jaw is prominent, the hands are large, and there is gynaecomastia on both sides. He also shows sinus bradycardia. Body hair has a feminine distribution. The testes are small and soft and a bi...

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