Results 51 to 60 of about 156,607 (160)
Transvaginal Strain Elastography Methodology in Deep Endometriosis
Journal of Ultrasound in Medicine, EarlyView.Objectives Transvaginal strain elastography (SE) has emerged as a complementary technique to transvaginal ultrasound for deep endometriosis (DE) evaluation by exploiting tissue stiffness between lesions and surrounding structures. However, its clinical adoption remains limited by marked methodological heterogeneity across studies.
Ana Claudia Brunelli Tosato +4 more
wiley +1 more source
Primary amenorrhea with transverse vaginal septum [PDF]
Transverse vaginal septum is a rare congenital anomaly with an incidence of 1:2100 due to incomplete fusion of mullerian duct and the urogenital sinus component of the vagina. Surgical management of the transverse vaginal septum is based on its thickness
Vaidya, Dakshaja +3 more
core +1 more source
Prenatal Diagnosis, EarlyView.ABSTRACT Objective This study describes the role of pre‐EXIT (Ex Utero Intrapartum Treatment) fetoscopic airway evaluation in fetuses with suspected airway obstruction. Methods Single center, retrospective, observational study including fetuses with suspected airway obstruction undergoing fetoscopic airway evaluation prior to EXIT between 2013 and 2025.
Daniel Sanin‐Ramirez +6 more
wiley +1 more source
Maternal Lead Exposure Induces Glandular Alterations in the Salivary Glands of Rat Male Offspring
Environmental Toxicology, EarlyView.ABSTRACT Lead (Pb) is a widely distributed environmental pollutant that is highly noxious due to its toxicokinetic characteristics. Pb exposure can damage vital organ systems, including the central nervous and stomatognathic systems. As salivary glands play an important role in oral homeostasis, this study aimed to investigate the effects of maternal ...
Rayssa Maitê Farias Nazário +8 more
wiley +1 more source
Ultrasound in Obstetrics &Gynecology, EarlyView.ABSTRACT Objective To characterize prenatal ultrasound findings in fetuses with prenatally diagnosed closed spinal dysraphism (CSD) and report their postnatal management and functional outcomes at 18 and 36 months. Methods This retrospective cohort study included all fetuses with a prenatal diagnosis of CSD assessed between January 2014 and December ...
Y. Athiel +15 more
wiley +1 more source
A Spotlight on Yolk‐sac Tumors: Molecular Pathology, Current Diagnostics, and Novel Therapeutics
Andrology, EarlyView.ABSTRACT Background Yolk‐sac tumors are an aggressive subtype of testicular cancer that significantly contribute to disease progression and therapy resistance, especially in adults. While testicular cancer generally has high cure rates with cisplatin‐based treatment, adult yolk‐sac tumors often appear as components of mixed tumors with poor response to
Evangelos Prokakis +3 more
wiley +1 more source
Septate uterus with cervical duplication and longitudinal vaginal septum: A two case series
Laparoscopic, Endoscopic and Robotic Surgery, 2019 Müllerian duct anomalies consist of a set of structural malformations resulting from abnormal development of the paramesonephric or Müllerian ducts. Failures in lateral fusion may result in uterus didelphys, bicornuate uterus or arcuate uterus while ...
Noa Ndoua Claude Cyrille +6 more
doaj +1 more source
Acta Paediatrica, EarlyView.ABSTRACT Aim This study aimed to investigate the incidence, risk factors and possible aetiology of sudden unexpected postnatal collapse (SUPC), a potentially fatal yet poorly understood event. Methods In a retrospective cohort, patient records from 483 284 infants born in Stockholm, Sweden, between 2002 and 2022 were screened for SUPC‐related diagnoses.
David Forsberg +5 more
wiley +1 more source
Uterus didelphys with double vagina diagnosed during third cesarean section: A case report
SAGE Open Medical Case Reports, 2022 Uterus didelphys is a rare uterine anomaly. It is associated with fetal breech presentation, preterm delivery, and cesarean section. Longitudinal vaginal septum may be associated with uterus didelphys, which may cause dyspareunia and labor obstruction ...
Namkha Dorji +2 more
doaj +1 more source
Clinical Genetics, EarlyView.Genetic causes of Müllerian aplasia remain largely unknown. We report the first molecularly confirmed case of Coffin–Siris syndrome 3 caused by a de novo SMARCB1 variant presenting with Müllerian aplasia, supporting a potential association between BAF complex dysfunction and abnormal Müllerian duct development. Created in BioRender. Herlin, M. K. (2026)
Anneli C. S. Bolund +5 more
wiley +1 more source