نتایج جستجو برای: triple x syndrome

تعداد نتایج: 1235406  

Journal: :Journal of Education and Work 2021

The further and higher educational experiences consequent employability of women with the under-researched Triple X syndrome are arguably unknown. This research study examines their special edu...

Journal: :European Journal of Human Genetics 2009

Journal: :Journal of Medical Genetics 1972

Journal: :The British journal of psychiatry : the journal of mental science 1963
C B KIDD R S KNOX D J MANTLE

Among recent developments in human chromosome studies a triple-X state has been recognized in females in whom the chromosome number is 47, composed of @ autosomes and 3 X chromosomes (Jacobs et al., 5959). Early surveys of nuclear sex have shown that the triple-X state is a not uncommon chromosomal anomaly. A survey of Edinburgh babies gave a frequency at birth of these abnormal females of 5 . ...

Journal: :گوارش 0
ahmad khodadad mehri najafi-sani fatemeh famouri v modaresi

allgrove syndrome also known as triple-a syndrome is an autosomal recessive disorder characterized by alacremia, achalasia and acth-resistant adrenal insufficiency. although this syndrome is rare, herein we report four cases with different clinical manifestations. they were referred to the gastrointestinal ward during a one year period with complaints of vomiting and dysphagia. the diagnosis of...

Journal: :The Journal of Pediatric Research 2018

Journal: :Journal of Human Reproductive Sciences 2011

Journal: :International Journal of Infertility & Fetal Medicine 2013

Journal: :gastroenterology and hepatology from bed to bench 0
baran parhizkar md nakisa maghsoodi mojgan forootan amirhosein entezari

triple a syndrome (allgrove syndrome) is a rare inherited autosomal recessive disease with a typical triad including adrenocorticotrophic-hormone-resistant glucocorticoid insufficiency, reduced or absent tearing (alacrima) and achalasia and a wide range of symptoms can be detected due to multi organ involvement. this report describes the case of a triple asyndrome, a12 year-old boy with a histo...

Journal: :Journal de gynecologie, obstetrique et biologie de la reproduction 2009
H Ben Hamouda N Mkacher H Elghezal H Bannour M Kamoun H Soua A Saad M M Souissi M T Sfar

Triple X syndrome is a relatively common sex chromosomal abnormality occurring in 0,1% of live-born female infants. Most of these infants have a normal phenotype and only a few cases with 47, XXX karyotype have congenital malformations. We report three cases of triple X syndrome that were diagnosed prenatally by genetic amniocentesis for advanced maternal age and have been observed from birth t...

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