The epidemiology of turner syndrome is largely unknown a few studies of prevalence and incidence of the syndrome have been performed based on large chromosome surveys, and based on these studies . Turner syndrome (ts) was first described in 1938, when dr henry turner observed a group of girls who all had the same unique physical features—short height, webbed necks, and undeveloped sex features because dr turner could see these features, they aren't truly symptoms—they are signs . Patients with turner syndrome may present with a cystic hygroma on a fetal ultrasound  or may have swollen hands and feet owing to lymphedema at birth children usually present with short stature, but some girls younger than 11 years have heights within the normal range for girls without turner .
Turner syndrome is a chromosomal condition related to the x chromosome that alters development in females, though it is not usually inherited in families symptoms of turner syndrome are: turner syndrome is a chromosomal condition that alters development in females women with this condition tend to . Turner syndrome (ts) is also known as turner's syndrome, 45,x syndrome, ullrich-turner syndrome, or gonadal dysgenesis what is turner syndrome turner syndrome is a chromosomal disorder. Most individuals with turner syndrome experience loss of ovarian function early in childhood, and thus do not enter puberty at the normal age turners syndrome consider clinical trials . Turner syndrome is a genetic condition caused by an abnormality on one of your sex chromosomes it is also called monosomy x turner syndrome is a genetic condition caused by an abnormality on one .
Turner syndrome (ts) is characterized by the absence of part of or the entire x chromosome in a woman, with typical stigmata like short stature, primary amenorrhea, estrogen insufficiency, and cardiovascular malformations. Turner syndrome, also referred to as ullrich-turner syndrome, is a genetic disorder in which an x chromosome is missing or structurally abnormal and is not caused by a growth hormone deficiency [ close window ]. A collection of disease information resources and questions answered by our genetic and rare diseases information specialists for turner syndrome. The study of turner syndrome (ts) has largely been based on smaller clinical studies and many case reports, since the initial descriptions by turner and ullrich , knowledge concerning any condition based on such data may introduce ascertainment bias, as seen in hospital based studies with patients skewed towards a more severe phenotype .
A diagnosis of turner syndrome is based upon identification of characteristic symptoms, a detailed patient history, a thorough clinical evaluation, and a variety of specialized tests turner syndrome should be suspected in girls with growth deficiency or short stature of unknown cause. Turner syndrome society of the united states ~ 11250 west rd suite g houston tx 77065 ~ 1- 800-365-9944 ~ [email protected] newly-updated ts clinical . Description turner syndrome is a chromosomal condition that affects development in females the most common feature of turner syndrome is short stature, which .
Je pinskerclinical review: turner syndrome: in patients with turner's syndrome and et alclinical and epidemiological description of aortic . Mosaicism 47,xxy/46,xx with clinical features suggestive of ks is very rare thus far, only about 10 cases have been described in literature turner syndrome . Description turner syndrome (ts) is a genetic condition that occurs in approximately 1/2500 live female births this clinical practice guideline uses evidence .
Definition/description parsonage–turner syndrome (pts) is the term used to describe a neuritis involving the brachial plexus, and is also referred to as idiopathic brachial plexopathy or neuralgic amyotrophy. Turner syndrome was first reported as a clinical syndrome (prior to the availability of karyotyping) in seven women with short stature, sexual immaturity, neck webbing, and cubitus valgus in a paper published in 1938 by henri turner, an oklahoma physician . The turner syndrome society offers education and support for all those touched by ts. In turner syndrome, which only affects females, there is a partially or completely missing x chromosome symptoms children with turner syndrome can be very different from one another, and symptoms vary greatly from child to child.