Protein associated with SMAD1 (PAWS1/FAM83G) is a substrate for type I bone morphogenetic protein receptors and modulates bone morphogenetic protein signalling [PDF]
, 2014 Bone morphogenetic proteins (BMPs) control multiple cellular processes in embryos and adult tissues. BMPs signal through the activation of type I BMP receptor kinases, which then phosphorylate SMADs 1/5/8.
Campbell, David +7 more
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Assessment and significance of long-term outcomes in pediatric surgery [PDF]
, 2017 Treatment modalities for newborns with anatomical congenital anomalies have greatly improved over the past decades, with a concomitant increase in survival. This review will briefly discuss specific long-term outcomes to illustrate, which domains deserve
Gischler, S.J. (Saskia) +3 more
core +4 more sources
Omphalocele and gastroschisis: comparison of outcome in a resource limited tertiary centre
Хірургія дитячого віку, 2018 Background. Neonates with gastroschisis are expected to have better prognosis than omphalocele as the latter is commonly associated with other congenital anomalies. But in our centre, we experience the opposite scenario regarding outcome. The aim of this
Samiul Hasan +4 more
doaj +1 more source
Primary versus Staged Closure of Exomphalos Major: Cardiac Anomalies Do Not Affect Outcome [PDF]
, 2018 Aim: The objective of the study is to describe management of exomphalos major and investigate the effect of congenital cardiac anomalies. / Methods: A single-center retrospective review (with audit approval) was performed of neonates with exomphalos ...
Cross, KMK +7 more
core
The acrocallosal syndrome: A case report and literature survey [PDF]
, 2009 Acrocallosal syndrome (ACS) is a rare, genetically transmitted disorder characterized by facial deformities. These include a large forehead, large anterior fontanelle, broad nasal bridge with increased intercanthal distance, partial or complete agenesis ...
Davies, Lindsey +2 more
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Perforated small bowel in omphalocele at birth
Journal of Indian Association of Pediatric Surgeons, 2006 The rupture of an omphalocele sac during birth is a well recognized entity. The associated lesions due to vascular compromise can result in necrosis of the bowel with perforation.
Kale R, Handa R, Harjai Man
doaj
Omphalocele in Both Twins: Revealing Developmental Complexities: A Case Report
Gynecology Obstetrics & Reproductive MedicineOmphalocele is a rare congenital anomaly with eviscerated abdominal organs in the proximal segment of the umbilical cord covered by a membranous sac. This case presents omphalocele in both fetuses in a twin pregnancy, discussing the embryological basis,
Sampath Gnanarathne, Ayodhya Kariyawasam
doaj +1 more source
Pregnancy with Didelphys Uterus and Omphalocele Infant: A Case Report [PDF]
, 2021 Leony Lim +3 more
openalex +1 more source
Beckwith Wiedemann Syndrome : presentation of a case report [PDF]
, 2008 Beckwith Wiedemann Syndrome (BWS) is a rare congenital disease of low prevalence. However, it presents a high prevalence within the genetic pathologies of overgrowth.
Fernández Toro, María de los Ángeles +3 more
core +1 more source
Congenital peritoneopericardial diaphragmatic hernia in a family of Persian cats
Journal of Feline Medicine and Surgery Open Reports, 2018 Case series summary The congenital midline defects of peritoneopericardial diaphragmatic hernia (PPDH) and omphalocele are believed to be related developmental defects, and have both been described in cats and dogs.
Carol Margolis +5 more
doaj +1 more source