Results 71 to 80 of about 167,430,042 (175)
, 2023 CJC Pediatric &Congenital Heart Disease, Volume 2, Issue 3, Page 162-165, June 2023.
wiley +1 more source
Prenatal multidisciplinary counseling for fetal congenital anomalies: A narrative review
International Journal of Gynecology &Obstetrics, Volume 169, Issue 2, Page 498-510, May 2025.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
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Routine 36‐week scan: diagnosis of fetal abnormalities
Ultrasound in Obstetrics &Gynecology, Volume 65, Issue 4, Page 427-435, April 2025.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
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Case report: Pentalogy of cantrell
The Egyptian Heart Journal, 2014 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
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Ectopia Cordis: A Case Report [PDF]
International Journal of Anatomy Radiology and Surgery, 2016 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
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Retrospective Study of Clinical and Genetic Profiles of Alpha‐Mannosidosis Patients From the UAE
JIMD Reports, Volume 66, Issue 2, March 2025.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
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Ventral body wall closure: Mechanistic insights from mouse models and translation to human pathology
Developmental Dynamics, Volume 254, Issue 2, Page 102-141, February 2025.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
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Scientific Reports, 2021 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
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CJC Pediatric &Congenital Heart Disease, Volume 4, Issue 1, Page 34-48, February 2025.Graphical abstract Abstract Factors such as physical activity (PA), sedentary time, screen time, and sleep affect the holistic health of children with congenital heart disease (CHD). Despite this, their proximity to reaching the Canadian 24‐hour movement guidelines is unknown.
Matthew S. Chapelski +7 more
wiley +1 more source
The umbilical cord in Cantrell: Pentalogy or Hexalogy?
, 2009 Objective: Pentalogy of Cantrell (PC) is a rare congenital defect associated with five midline anomalies. The type of cardiac malformation and the size of the abdominal wall defect is often responsible for the high mortality.
Tutschek, Boris +3 more
core +1 more source