Results 51 to 60 of about 550 (151)
ABSTRACT Introduction Palpitations in children are common and obtaining symptom‐rhythm correlation is diagnostic, but challenging to obtain. The AliveCor KardiaMobile monitor is a smartphone‐based single‐lead ECG event recorder with limited study in children.
Hilal Al Riyami +7 more
wiley +1 more source
Prenatal multidisciplinary counseling for fetal congenital anomalies: A narrative review
Abstract Introduction Prenatal multidisciplinary counseling for fetuses with congenital anomalies involves a collaborative approach, integrating expertise from various medical fields. Aims and Approach This comprehensive strategy aims to provide expectant parents with accurate information about the diagnosis, potential outcomes, and available ...
Licia Lugli +10 more
wiley +1 more source
Routine 36‐week scan: diagnosis of fetal abnormalities
ABSTRACT Objectives To investigate further the incidence and types of fetal abnormality identified at a routine 36‐week ultrasound examination, which had not been diagnosed in previous scans at 20 weeks and 12 weeks' gestation, and to report the fetal abnormalities that are diagnosed only postnatally.
A. Syngelaki +5 more
wiley +1 more source
Case report: Pentalogy of cantrell
Pentalogy of Cantrell is a type of ectopia cordis including: defect in anterior diaphragm, pericardium, anterior abdominal wall in addition to extrusion of part of the heart outside the mediastinum and structural heart disease. We were faced by a case of
Al sayed salem
doaj +1 more source
Ectopia Cordis: A Case Report [PDF]
Pentalogy of Cantrell is a rare a congenital syndrome which includes ectopia cordis, sternal, pericardial, abdominal wall defects (usually omphalocele), diaphragmatic defects and intracardiac abnormalities. We report a case with a rare combination of
Muhammad Abdullah, R. Ramesh Kumar
doaj +1 more source
Retrospective Study of Clinical and Genetic Profiles of Alpha‐Mannosidosis Patients From the UAE
ABSTRACT Alpha‐mannosidosis (AM; OMIM 248500) is a rare autosomal recessive lysosomal storage disorder caused by mutations in MAN2B1, which codes for the lysosomal alpha‐mannosidase enzyme (LAMAN; EC:3.2.1.24). Clinical characteristics include developmental delay, hearing impairment, and recurrent infections.
Ali K. Saad +6 more
wiley +1 more source
Ventral body wall closure: Mechanistic insights from mouse models and translation to human pathology
Abstract The ventral body wall (VBW) that encloses the thoracic and abdominal cavities arises by extensive cell movements and morphogenetic changes during embryonic development. These morphogenetic processes include embryonic folding generating the primary body wall; the initial ventral cover of the embryo, followed by directed mesodermal cell ...
Caroline Formstone +3 more
wiley +1 more source
No studies of the efficacy and safety of surgical techniques for the primary closure of giant omphalocele have been performed in Colombia. To determine the mortality rate and factors associated with mortality in neonates with giant omphalocele subjected ...
Alexander Barrios-Sanjuanelo +2 more
doaj +1 more source
Clinical and Surgical Perspectives on Isolated Thoracic Ectopia Cordis: A Rare Case Report
Ectopia cordis is an exceptionally uncommon congenital condition where the heart develops outside its normal position due to incomplete closure of the ventral chest wall during embryogenesis. The anomaly may occur in isolation or with other structural defects, often resulting in a poor prognosis despite advancements in medical and surgical care.
Syed Mohsin Raza Bukhari +9 more
wiley +1 more source
Introducción: la Pentalogía de Cantrell (PC) se compone de cinco anomalías: defecto superior de pared abdominal, defecto esternal inferior, defecto diafragmático anterior, defecto pericárdico diafragmático y anormalidades del corazón.
Harry Pachajoa
doaj +3 more sources

