Search results
Results from the WOW.Com Content Network
Henry Turner. Turner syndrome (TS), also known as 45,X, or 45,X0, is a genetic disorder in which cells have only one X chromosome or are partially missing an X chromosome (sex chromosome monosomy) leading to the complete or partial deletion of the pseudoautosomal regions (PAR1, PAR2) in the affected X chromosome. [2][6][7] Most people have two ...
Turner's hypoplasia or Turner's tooth is a presentation of enamel hypoplasia that normally affects only a single tooth. Its causes can be the same as other forms of enamel hypoplasia, but it is most commonly associated with trauma to a primary maxillary central incisor and the subsequent developmental disturbance of the underlying permanent ...
Frequency. 1 in 1000 (1 in 2,000 severe disease) [4] Named after. Jacqueline Noonan. Noonan syndrome (NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems, and skeletal malformations. [1] Facial features include widely spaced eyes, light-colored eyes, low-set ...
Turner ultimately became one of the top box-office draws, and most sought-after actresses of the 1980s and early 1990s. Turner stated in 2018, "Body Heat was a blessing because I went straight to being a leading actor and I didn't have to suffer any of this predatory male behaviour like many young actresses. It doesn't frustrate me that nearly ...
2. Henry Hubert Turner (August 28, 1892 – August 4, 1970) was an American endocrinologist, noted for his published description of Turner syndrome in 1938 at the annual meeting of the Association for the Study of Internal Secretions. He served as chief of endocrinology and as associate dean of the University of Oklahoma College of Medicine.
Webbed neck. Webbed neck. Other names. Pterygium colli deformity. Teenage girl with Turner syndrome and webbed neck. Specialty. Medical genetics. A webbed neck, or pterygium colli, is a congenital skin fold that runs along the sides of the neck down to the shoulders. There are many variants.
Parsonage–Turner syndrome, also known as acute brachial neuropathy, neuralgic amyotrophy and abbreviated PTS, is a syndrome of unknown cause; although many specific risk factors have been identified (such as; post-operative, post-infectious, post-traumatic or post-vaccination). [4] It is also known as brachial plexitis, and results in ...
approximately 1 in 1,000 (female) Trisomy X, also known as triple X syndrome and characterized by the karyotype [ note 1 ]47,XXX, is a chromosome disorder in which a female has an extra copy of the X chromosome. It is relatively common and occurs in 1 in 1,000 females, but is rarely diagnosed; fewer than 10% of those with the condition know ...