Zobrazeno 1 - 10
of 231
pro vyhledávání: '"Mullerian agenesis"'
Autor:
Monika Gautam, Meenakshi Chauhan, Vani Malhotra, Sushila Chaudhary, Sarika Gautam, Menka Verma
Publikováno v:
Asian Journal of Medical Sciences, Vol 15, Iss 8, Pp 179-181 (2024)
Mullerian duct anomalies are developmental anomalies resulting from failure in organogenesis, fusion, or the reabsorption of the paired Mullerian ducts. Endometriosis and Mullerian anomalies have a high coincidence rate. Obstructive uterine malformat
Externí odkaz:
https://doaj.org/article/8bf0ef99532c4b0c9011a43e46d580a5
Autor:
Shriya Devendra Tayade, Nadia Mehdi, Rajani Dube, Vaishnavi Bose, Ashna Ameer, Zainabsadat Tabatabaei Hakim, Arnaud Wattiez
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-6 (2024)
Abstract Introduction Menstruation is a developmental milestone and usually marks healthy and normal pubertal changes in females. Menarche refers to the onset of first menstruation in a female. The causes of primary amenorrhea include outflow tract a
Externí odkaz:
https://doaj.org/article/f1b71b608e384bb0a4dc413deb210c8c
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 Ovarian Research, Vol 16, Iss 1, Pp 1-6 (2023)
Abstract Background Herniation of ovaries and Mullerian structures into inguinal canal is usually reported in infants and is rare among adults. We are presenting a rare case of Mullerian agenesis and Turner mosaic syndrome with tubo-ovarian inguinal
Externí odkaz:
https://doaj.org/article/0836af46117449158cb17e0ac0da6208
Publikováno v:
Majallah-i Zanān, Māmā̓ī va Nāzā̓ī-i Īrān, Vol 25, Iss 11, Pp 98-102 (2023)
Introduction: Uterine anomalies have been caused by impairment in the formation, evolution, or defect in the connection of Mullerian bud during the embryonic period. In this study, a case of unicornuate uterus with cervical agenesis is presented. Cas
Externí odkaz:
https://doaj.org/article/20df3fc9ef844330a1771660b3e6df53
Akademický článek
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Autor:
Rohan Kumar Singh, Prerna Anup Patwa, Gaurav Vedprakash Mishra, Rajasbala Pradeep Dhande, Suresh Vasant Phatak, K. B. Harshith Gowda
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 53, Iss 1, Pp 1-4 (2022)
Abstract Introduction Meyer–Rokitansky–Küster–Hauser syndrome is rare congenital abnormality in females with a blind ending vagina. There can be associated hypoplasia of uterus. The syndrome is of sporadic origin and affects the reproductive l
Externí odkaz:
https://doaj.org/article/87b36f87f48a4d0cbc9b1b3bb6001335
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Rahul Saini, Lovenish Bains, Tarangpreet Kaur, Pawan Lal, Veer Pal, Mohd Yasir Beg, Daljit Kaur
Publikováno v:
Journal of Ovarian Research, Vol 14, Iss 1, Pp 1-6 (2021)
Abstract Background Inguinal hernia containing ovary and fallopian tube can be found in paediatric population and is a rare finding in women of reproductive age group. Most of the cases are associated with congenital abnormalities of the female genit
Externí odkaz:
https://doaj.org/article/c5b23f2b0ba44c03a3ce6745d8db6211
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 9, Iss 8, Pp 3986-3990 (2020)
Context: Primary Amenorrhea is worrisome for the adolescent as well as their guardian. It is essential to be able to identify the underlying pathology and initiate appropriate management strategies, well in time. Aims: To study the clinical features,
Externí odkaz:
https://doaj.org/article/d295ceddb501455f8b6738eed7666cfc