Results 51 to 60 of about 1,121,512 (150)

Septate uterus with cervical and vaginal duplication: A rare Mullerian malformation

Medical Journal of Dr. D.Y. Patil University, 2013
A rare case of Mullerian anomaly in a 26-year-old woman who presented with recurrent pregnancy loss and was found to have a longitudinal vaginal septum with cervical duplication and two endometrial cavities separated by a complete septum.
Meenal Patvekar, Vinayak Mahajan, Gazal Garg   +2 more
doaj   +1 more source

Prospective echocardiographic characterization of postnatal cardiac development in C57BL/6 mice: Strain analysis between birth and adulthood

Physiological Reports, Volume 14, Issue 18, September 2026.
Abstract Echocardiography is critical for characterizing murine models of cardiovascular disease, yet normative data for the early postnatal period, particularly advanced functional metrics like myocardial strain, remain undefined. This developmental window features rapid cardiac maturation and is central to modeling congenital and neonatal heart ...
Sehjin Jo, George Spyropoulos, Logan G. Hart, Taylor A. Covington, Arvind K. Pandey, Thomas Michel, Fotios Spyropoulos   +6 more
wiley   +1 more source

Herlyn-Werner-Wunderlich syndrome also known as obstructed hemivagina and ipsilateral renal anomaly: A case report and a comprehensive review of literature

Radiology Case Reports, 2023
Herlyn-Werner-Wunderlich syndrome, also known as obstructed hemivagina and ipsilateral renal anomaly (OHVIRA), is a Müllerian duct anomaly. It is a rare clinical condition consisting of a duplicated uterus with an oblique vaginal septum that causes ...
André Luís Borges, MD, Nhalim Sanha, MD, Helena Pereira, MD, Ana Martins, MD, Cristina Costa, MD   +4 more
doaj   +1 more source

Managing TRAP Sequence Conservatively: A Case Report of Full‐Term Pregnancy With Favorable Outcome

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Acardiac twinning, also known as Twin reversed arterial perfusion (TRAP) sequence, is a rare anomaly seen exclusively in monochorionic twin pregnancies. It occurs due to abnormal placental vascular anastomoses, allowing retrograde perfusion from healthy “pump” twin to severely malformed twin lacking a functional heart.
Bishal Khaniya, Ayush Shrestha, Anish Sah, Rita Adhikari, Sujata Bhandari, Aashish Bhandari, Ram Aryal, Sameep Sapkota, Puspa Raj Bham, Madhur Bhattarai   +9 more
wiley   +1 more source

Case Report With Biallelic Variants in GCNT2 Implicates Exon 1B in Congenital Cataracts

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1716-1718, July 2026.
ABSTRACT GCNT2‐related cataracts is a disorder characterized by bilateral congenital cataracts (CC) of various types (with or without the adult i blood phenotype) and is caused by biallelic variants in GCNT2, which has 3 major isoforms, differentiated by alternative splicing of the first exon (known as exon 1A, B, and C).
Audrey O'Neill, Cindy Bayer, Emily McQuillen, Erica D. Smith, Meghan Towne, Dallas Reed   +5 more
wiley   +1 more source

Septate uterus with cervical duplication and a longitudinal vaginal septum: an unclassified mullerian anomaly [PDF]

, 2016
Uterine anomalies are the result of disturbances in the development, formation or fusion of the mullerian ducts during foetal life with an incidence of 0.001%-10% in general population.
Mangla, Ruchika, Kaur, Tajinder, Pathak, Nayana   +2 more
core   +1 more source

Is Hysteroscopic Metroplasty Advisable for U2bC2V1 Malformation?

Diagnostics
A complete uterine septum, with a double cervix and vaginal septum, is a complex and rare congenital genital tract anomaly. The diagnosis is difficult and often challenging, requiring complex imaging investigations and diagnostic hysteroscopy.
Iulian Gabriel Goidescu, Adelina Staicu, Alexandra-Andreea Poienar, Mihai Surcel, Romeo Micu, Dan Boitor Borza, Daniel Muresan   +6 more
doaj   +1 more source

From Behavioral and Sleep Disturbances to Genetic Diagnosis: Smith–Magenis Syndrome and the Importance of the Diagnostic Pathway

Developmental Neurobiology, Volume 86, Issue 3, July 2026.
ABSTRACT Smith–Magenis syndrome (SMS) is a rare multisystem genetic disorder caused by a 17p11.2 microdeletion or pathogenic variants in the retinoic acid‐induced 1 (RAI1) gene. It is characterized by developmental delay, distinctive craniofacial features, behavioral dysregulation, and inverted sleep–wake rhythm.
Fethiye Kılıçaslan, Ayşe Rümeysa Olgar Çetin, Özlem Öz, Mert Coşkun, Mehmet Burak Mutlu, Berna Polat Tüysüz   +5 more
wiley   +1 more source

Leiomyoma on the septum of a septate uterus with double cervix and vaginal septum: a challenge to manage

, 2008
Objective: To describe the first case of a leiomyoma localized in the septum of a septate uterus that had cervical duplication and a longitudinal vaginal ...
ÇORAKÇI, AYDIN, Turkoz, Erkan, Caliskan, Eray, Cakiroglu, Yigit   +3 more
core   +1 more source

Management of mullerian development anomalies: 9 years' experience of a tertiary care center

Gynecology and Minimally Invasive Therapy, 2020
Objectives: This study aimed to analyze the clinical and imaging findings as well as the outcomes of patients with Mullerian duct anomalies. Materials and Methods: A retrospective analysis of 41 patients with Mullerian development anomalies treated in a ...
Lajya Devi Goyal, Balpreet Dhaliwal, Paramdeep Singh, Sandesh Ganjoo, Vikas Goyal   +4 more
doaj   +1 more source