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Clinical case of disorder of sex development, 46 XY, SRY+

Bulletin of Reproductive Health
People, who born with disorders/differences of sex development (hereinafter -DSD) represent a special cohort of patients, because their observation and treatment requires the cooperative work of endocrinologists, gynecologists, surgeons and psychologists.
V. D. Ankina   +3 more
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Simpson–Golabi–Behmel syndrome with 46,XY disorders of sex development: A case report

American Journal of Medical Genetics Part A, 2019
AbstractWe present a case of a Chinese child with X‐linked Simpson–Golabi–Behmel syndrome (SGBS). To the best of our knowledge, this is the first report of 46,XY disorders of sex development (ambiguous genitalia, cryptorchidism, and uterus in the pelvis) in surviving SGBS patients.
Qian Fu, Hui Wang, Zhan Qi, Yaxin Zhang
openaire   +2 more sources

Prostate Screening in Patients With 46,XY Disorders of Sex Development—Is it Necessary?

Journal of Urology, 2008
We used current methods of screening for prostate cancer, digital rectal examination and serum prostate specific antigen as an initial assessment of risk in a young group of adult 46,XY patients affected by disorders of sex development.Adult intersex patients older than 21 years, under long-term followup at the Pediatric Endocrinology Clinic of the ...
Amirali Hassanzadeh, Salmasi   +5 more
openaire   +2 more sources

A Study of Gender Outcome of Egyptian Patients with 46,XY Disorder of Sex Development

Sexual Development, 2010
Children with disorder of sex development (DSD) may be born with ambiguous genitalia. Decision-making in relation to sex assignment has been perceived as extremely disturbing and difficult to families and health care professionals. This is mainly due to a general paucity of information about the condition and an exaggerated feeling of stigma and shame ...
S I, Ismail, I A, Mazen
openaire   +2 more sources

Novel mutations of HSD17B3 in three Chinese patients with 46,XY Disorders of Sex Development

Steroids, 2017
17β-Hydroxysteroid dehydrogenase type 3 (17β-HSD3) converts the inactive Δ4-androstenedione (A) to testosterone (T). Its deficiency is the most common testosterone biosynthesis defect that results in 46,XY Disorders Of Sex Development (DSD). However, the disease is difficult to distinguish from other 46,XY DSD for similar clinical phenotypes. Therefore,
Bingqing, Yu   +12 more
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Phalloplasty: A Panacea for 46,XY Disorder of Sex Development Conditions with Penile Deficiency?

2014
In cases of severe penile inadequacy, such as in pathological conditions involving penile amputation (e.g. penile cancer), or in 46,XY disorders of sex development with severe undervirilization or maldevelopment of the penis (e.g. idiopathic micropenis, cloacal exstrophy), standard (surgical) penile lengthening techniques do not provide patients with a
Nina, Callens, Piet, Hoebeke
openaire   +2 more sources

46 XY disorder of sex development: case report

Journal of Pediatric Urology, 2020
Harry Achsan Chaerul   +2 more
openaire   +1 more source

46 xy disorders of sex development (dsd): a case report

Endocrine Abstracts, 2023
Farah Elgharroudi   +2 more
openaire   +1 more source

Clinical and Biochemical Profile of Patients with 46, XY Disorders of Sex Development

QJM: An International Journal of Medicine
Abstract Background Disorders of sex development (DSD) comprise a wide range of conditions with varying features and pathophysiology that most often present in the newborn or the adolescent. Affected newborns are born with ambiguous genitalia, whereas adolescents present with atypical sexual ...
Nagwa Mosaed Hassan Ali   +3 more
openaire   +1 more source

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