Results 61 to 70 of about 270,220 (169)
ABSTRACT Congenital hypogonadotropic hypogonadism (CHH) is a rare group of disorders of gonadotropin deficiency, either isolated or as a part of multiple pituitary hormone deficiencies (MPHD). We aimed to describe the spectrum of presentation, diagnosis, and management practices of CHH spanning 30 years at an Australian tertiary paediatric centre. This
Minha Kook +3 more
wiley +1 more source
Uterine Rupture in a Primigravida with Mullerian Anomaly at 27 Weeks Gestation [PDF]
Mullerian anomalies are rare and are often associated with infertility, chronic pelvic pain and pregnancy wastage. This is a case report of a primigravida at 27 weeks gestation, who presented in shock.
Kosgei, RJ +3 more
core +1 more source
Müllerian duct anomalies: review of current management
The aim of this paper was to discuss the embryological aspects of Müllerian duct anomalies and to analyze the current diagnostic methods and therapy. Müllerian anomalies are congenital defects of the female reproductive tract resulting from failure in ...
Sérgio Conti Ribeiro +6 more
doaj +1 more source
Abstract To describe clinical presentation and genetic findings in a cohort of infants with congenital hypogonadotropic hypogonadism (CHH) diagnosed before 2 years of age. From a large cohort of patients who underwent next‐generation sequencing (NGS) for CHH between 2019 and 2025, we identified all patients tested at ≤2 years of age.
Karine Aouchiche +16 more
wiley +1 more source
Management of Second Trimester Fetal Demise in a Noncommunicating Uterine Horn
Müllerian anomalies are uncommon but when present they can increase the risk of obstetrical complications. Anomalies such as bicornuate and unicornuate uterus can also increase the surgical risks of pregnancy termination.
R. Tyler Hillman +2 more
doaj +1 more source
Jacobs Syndrome Presenting With Delayed Puberty and Central Hypogonadism: A Rare Case Report
ABSTRACT In some rare instances, patients with 47,XYY syndrome can be short in height, accompanied by hypogonadism without the characteristic tall stature. In cases where there is delayed puberty and unusual growth pattern, a complete endocrine work‐up, including GnRH and hCG stimulation tests, along with chromosome studies, is vital.
Muhammad Hassaan Javaid +4 more
wiley +1 more source
Mullerian anomalies: a cause of primary amenorrhea [PDF]
Background: The objectives of this study were to determine the etiologic causes of amenorrhea, the prevalence of müllerian anomalies as a cause of primary amenorrhea and the different varieties of müllerian anomalies causing primary amenorrhea.Methods ...
Nakum, Kanaklata +3 more
core
This comprehensive review highlights the transformative role of 3D printing and bioprinting technologies in the regeneration of female reproductive organs and the treatment of gynecological diseases. Unlike previous overviews that focus narrowly on isolated applications, this work provides an integrative analysis of recent clinical and preclinical ...
Chan Hum Park, In‐Sun Hong
wiley +1 more source
Incidence of Incidental Finding of Mullerian Anomalies at Successful Term Pregnancies: A Three-Year Study in India [PDF]
Introduction: Mullerian Anomalies are known to disturb the reproductive life of women immensely and adversely affect their obstetric outcomes too. Therefore, they get identified either during pubertal, early reproductive or antenatal period.
Rai, Suvarna +3 more
core
External validation of anti-Müllerian hormone based prediction of live birth in assisted conception [PDF]
<p>Background - Chronological age and oocyte yield are independent determinants of live birth in assisted conception. Anti-Müllerian hormone (AMH) is strongly associated with oocyte yield after controlled ovarian stimulation.
Grisendi, V. +6 more
core +1 more source

