Results 51 to 60 of about 9,287 (208)

A successful in vitro fertilization outcome in a hermaphrodite male

open access: yes
International Journal of Gynecology &Obstetrics, Volume 169, Issue 1, Page 424-425, April 2025.
Shima Elbakhit M. E. Albasha   +2 more
wiley   +1 more source

Exploring hemodynamic alterations in gastroschisis: insights into fetal growth restriction using prenatal MRI

open access: yesUltrasound in Obstetrics &Gynecology, Volume 67, Issue 6, Page 795-805, June 2026.
Abstract Objective Despite the high incidence of fetal growth restriction (FGR) in gastroschisis (GS) associated with placental fetal vascular malperfusion (FVM), the underlying mechanism remains unclear. We aimed to investigate whether umbilical vein (UV) stenosis at the abdominal wall defect impairs fetoplacental circulation, leading to FGR.
H. Shi   +8 more
wiley   +1 more source

Phenotypic Clues in Infantile‐Onset Parkinsonism‐Dystonia‐2: A Treatable Neurotransmitter Disorder

open access: yes
Movement Disorders Clinical Practice, EarlyView.
Sangeetha Yoganathan   +10 more
wiley   +1 more source

Incidental Paratubal Non‐Functional Adrenal Rest in an Adult Female: A Rare Histopathological Finding

open access: yesClinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Paratubal adrenal rests, although rare in adult females, should be considered during histopathological evaluation of adnexal tissues, as they may mimic neoplasms or rarely undergo functional or pathological change. Surgeons should be aware of this possibility to avoid unnecessary concern or overtreatment when encountering small yellow nodules ...
Amir Hosein Jafarian   +3 more
wiley   +1 more source

Preoperative Manual Detorsion in Children With Intravaginal Testicular Torsion: A Single‐Center Experience

open access: yes
World Journal of Surgery, EarlyView.
Maria Ruffoli   +8 more
wiley   +1 more source

Genetic Characterization and Multidisciplinary Management of Complete Androgen Insensitivity Syndrome: Unveiling a Novel AR Mutation

open access: yesClinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT A novel AR frameshift mutation (c.2023_2035del) was identified in a 17‐year‐old phenotypic female with Complete Androgen Insensitivity Syndrome (CAIS). This report emphasizes the necessity of molecular characterization and multidisciplinary management to address diagnosis, surgical timing, and psychological well‐being in disorder of sex ...
Maria Francesca Astorino   +10 more
wiley   +1 more source

Prospective study on Surgical Management of Undescended Testis in a Tertiary Hospital [PDF]

open access: yes, 2020
INTRODUCTION: Undescended testis is one of the most common surgical problems encountered among paediatric age group. Undescended testis, age of diagnosis plays important role in outcome.
Praveenkumar, C P
core  

Yield of Whole Genome Sequencing for Pathogenic Single Nucleotide Variants in Congenital Heart Disease: A Systematic Review and Meta‐Analysis

open access: yesPrenatal Diagnosis, Volume 46, Issue 5-6, Page 780-818, May 2026.
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa   +7 more
wiley   +1 more source

Polyorchidism presenting with undescended testis

open access: yes, 2004
We report on a case of polyorchidism that presented as undescended testis. Polyorchidism is defined as the presence of more than two testes. As in our case, most cases occur on the left side.
Salman, FT   +3 more
core   +1 more source

Evolving Features of RASopathies Among Pregnancies With Abnormal Fetal Fluid Collections

open access: yesPrenatal Diagnosis, Volume 46, Issue 5-6, Page 892-903, May 2026.
ABSTRACT Objective We aimed to characterize the fetal features across gestation and describe genotype‐phenotype correlations for pregnancies with fetal RASopathies that were more severely affected as they presented with at least one abnormal fluid collection.
Natalie B. Gulrajani   +17 more
wiley   +1 more source

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