Morphological Changes of Amygdala in Turner Syndrome Patients
نویسندگان
چکیده
منابع مشابه
Morphological Changes of Amygdala in Turner Syndrome Patients.
AIMS Turner's syndrome (TS) losts one of the X chromosomes and exhibits social cognition deficits. Previous studies have reported that women with TS demonstrated structural and functional abnormalities in brain, including increased volume in amygdala. However, most studies regarded the amygdala as a whole, and the abnormalities in the specific subregions of amygdala in TS have not been studied....
متن کامل[Turner syndrome: the patients' view].
OBJECTIVE To identify how patients with Turner syndrome perceive their condition. METHODS Thirty-six women with Turner syndrome, aged between 15 and 25 years and with over 2 years of medical follow-up, were individually interviewed about: the impact of Turner syndrome at the moment of the diagnosis, their understanding of the syndrome, its effect in their lives, and their expectations for the...
متن کاملDental features in patients with Turner syndrome.
AIM This was to investigate the dental characteristics (caries sensitivity and tooth crown size of permanent elements) in subjects affected by Turner Syndrome (TS). PATIENTS AND METHODS A group of 25 patients affected by TS, aged from 4 to 18 years, was selected and the data were compared to those of an age matched control healthy group. The caries index values in TS patients are higher in th...
متن کاملEvaluation of Bone Changes in Patients with Pseudoexfoliation Syndrome
Purpose: To evaluate the association of osteoporosis and pseudoexfoliation syndrome. Methods: This case-control observational study was conducted on patients admitted to Baghaee Poor eye clinic of Shahid Sadoughi Hospital, Yazd, in 2015. The case group included 35 patients diagnosed with pseudoexfoliation syndrome and the control group included 35 patients with no evidence of pseudoexfoliation ...
متن کاملEffects of Karyotype Variations on Phenotype of Patients with Turner Syndrome
Background: Turner syndrome (TS) is a sporadic disorder caused by the absence of all or some parts one X-chromosome with major developmental consequences such as short stature and ovarian failure etc. The minor manifestations of TS are cubitus valgus, micrognatism, high-arched palate, short and/or webbed neck, hypothyroidism, etc. Different karyotype abnormalities may lead to different clinical...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: CNS Neuroscience & Therapeutics
سال: 2016
ISSN: 1755-5930
DOI: 10.1111/cns.12482