Zobrazeno 1 - 10
of 256
pro vyhledávání: '"primary amenorrhoea"'
Publikováno v:
Journal of Obstetrics and Gynaecology, Vol 44, Iss 1 (2024)
Background Primary amenorrhoea (PA) refers to an ailment when adolescent girls do not attain menarche naturally. It is one of the most common gynaecological disorders specified. Chromosomal abnormalities play a pivotal role in PA. Cytogenetic analysi
Externí odkaz:
https://doaj.org/article/a55da09805db453cb09b435a99ac553b
Publikováno v:
Bangabandhu Sheikh Mujib Medical University Journal, Vol 17, Iss 3 (2024)
Not available
Externí odkaz:
https://doaj.org/article/a401a0de158440e3a0398c97985ceb53
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 54, Iss 1, Pp 1-8 (2023)
Abstract Background This study aims to characterize the spectrum of imaging findings in patients of Mayer–Rokitansky–Kuster–Hauser (MRKH) syndrome presenting with primary amenorrhoea. Objectives (1) To aid in clinical diagnosis of MRKH syndrome
Externí odkaz:
https://doaj.org/article/ca422d286feb4cb68b86b2b79be35f10
Publikováno v:
Journal of Human Reproductive Sciences, Vol 15, Iss 2, Pp 187-190 (2022)
Background: Amenorrhoea is considered a kind of menstrual disorder in a woman of reproductive age. It is a symptom with many potential causes such as an abnormality in the hypothalamic–pituitary–ovarian axis, anatomical abnormalities of the genit
Externí odkaz:
https://doaj.org/article/1fa5b9f9b77c49fd95e5411b50b9fd18
Publikováno v:
Menopause Review, Vol 20, Iss 3, Pp 158-161 (2021)
Diagnosis of complete XY gonadal dysgenesis exposes the patient to the prospect of infertility and many years of medical treatment in order to avoid the development of diseases associated with this condition. However, sufficiently early diagnosis fol
Externí odkaz:
https://doaj.org/article/20b14f45ba2b4f258019893ba39c21cc
Publikováno v:
Journal of Human Reproductive Sciences, Vol 15, Iss 3, Pp 318-320 (2022)
Rearranged X chromosomes in Turner syndrome (TS) generally present with a mild phenotype, but in cases of ring X chromosomes, the incidence of intellectual disability and other congenital abnormalities can be significantly higher depending on the siz
Externí odkaz:
https://doaj.org/article/99dd04a88e3448729aa931c596241315
Autor:
Mohammad Moin Shahid
Publikováno v:
Sri Lanka Journal of Diabetes Endocrinology and Metabolism, Vol 10, Iss 1, Pp 30-33 (2020)
Mayer-Rokitansky-Haüser-Kuster (MRHK) or Mullerian agenesis syndrome is characterized by aplasia or hypoplasia of uterus and upper 2/3 of the vagina. Patients usually have normal gonadal function as both ovaries develop from different embryonic sour
Externí odkaz:
https://doaj.org/article/2174ced74cf04d48abd78884300dd826
Autor:
VELICHETI SANDEEP, BELLAMKONDA SANTH KUMAR, PADAVALA SATISH, B JAGADEESH KUMAR, PYLA SUDHA RANI
Publikováno v:
International Journal of Anatomy Radiology and Surgery, Vol 9, Iss 2, Pp 01-04 (2020)
Introduction: Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital anomaly in female genital tract owing to irregular embryonic development of para-mesonephric ducts and thus leads to uterine and proximal vagina aplasia or hypoplasia. M
Externí odkaz:
https://doaj.org/article/98257028d3e5437fa8a5f9b41bae9123
Publikováno v:
Acta Medica Lituanica, Vol 28, Iss 2 (2021)
During the development of the female genital tract, any insult to the normal development process results in a set of intriguing abnormalities known as Müllerian duct abnormalities. The uterine didelphys is the second least common type of anomaly amo
Externí odkaz:
https://doaj.org/article/5b9c748deb8d4f4c8a210308e19511c7
Autor:
Surendra, Vinu Choudhary
Publikováno v:
New Indian Journal of OBGYN, Vol 5, Iss 2, Pp 150-153 (2019)
The diagnosis and management of adolescent gynaecological conditions demands the need for dedicated teams to manage this complex group of transitional population between pediatric and adult age group. Primary amenorrhoea is one such condition that ca
Externí odkaz:
https://doaj.org/article/fc44bec593da409faad7616bd607159c