Results 111 to 120 of about 283,817 (266)
Unraveling the Role of WDR91: Case Report of a Previously Unrecognized Clinical Entity
Clinical Genetics, EarlyView.A novel case is herein described to expand the genetic and clinical spectrum of WDR91 and characterize a previously unrecognized autosomal recessive neurodevelopmental disorder. WDR91 deficiency results in neuronal loss, cortical thinning, and impaired brain development.
Nikolaos M. Marinakis +14 more
wiley +1 more source
Concurrent Mesh Repair of a Morgagni and Umbilical Hernia during a Laparoscopic Sleeve Gastrectomy in a Morbidly Obese Individual [PDF]
Journal of Krishna Institute of Medical Sciences University, 2016 Morgagni Hernia is a rare form of diaphragmatic hernia. It is mainly asymptomatic and often identified incidentally during surgery. Tension-free synthetic mesh repair is the preferred treatment modality.
N.R Kosai +4 more
doaj
Arthrogryposis: A Rare Manifestation in Infant of Diabetic Mother [PDF]
, 2009 Arthrogryposis multiplex congenita is characterized by non-progressive, multiple joint contractures present at birth. The major cause of arthrogryposis is fetal akinesia due to fetal abnormalities like neurogenic, muscle, connective tissue abnormalities ...
Kumar, Arvind +2 more
core
Diabetes, Obesity and Metabolism, EarlyView.Abstract Aims This randomised controlled trial compared the efficacy of modified laparoscopic sleeve gastrectomy with fundoplication (LSGFD) versus standard laparoscopic sleeve gastrectomy (LSG) in achieving weight loss and alleviating gastroesophageal reflux disease (GERD) in patients with obesity.
Pierdiwasi Maimaitiyusupu +5 more
wiley +1 more source
International Journal of Urology, EarlyView.ABSTRACT Recurrent ureteropelvic junction obstruction presents significant surgical challenges due to fibrosis, altered anatomy, and impaired vascularity. Open redo pyeloplasty has traditionally been the gold standard; however, it is associated with considerable morbidity.
Daisuke Ishii +4 more
wiley +1 more source
Pentalogy of Cantrell : the first Maltese case with successful outcome [PDF]
, 1997 Pentalogy of Cantrell is a rare disorder which was first described by Cantrell and his colleagues in 1958. It is comprised of congenital heart disease and midline defects.
Grech, Victor E. +2 more
core
Germ cell and other tumors in individuals with differences in sex development
CA: A Cancer Journal for Clinicians, EarlyView.Abstract Approximately one in 3500 to one in 5100 live‐born infants have atypical external genital development, known as differences in sex development (DSD). In 2005, an expert consensus conference thoroughly reviewed aspects of health care for individuals with DSD.
Selma Feldman Witchel +1 more
wiley +1 more source
Maternal complications following endoscopic surgeries in fetal Medicine [PDF]
, 2010 OBJETIVO: descrever as complicações maternas decorrentes dos procedimentos endoscópicos terapêuticos em Medicina fetal, realizados em um centro universitário no Brasil.
BARINI, Ricardo +6 more
core +2 more sources