Results 31 to 40 of about 1,787 (141)
Reparación de ectopia cordis asociada con pentalogía de Cantrell, presentación de un caso
Resumen: La pentalogía de Cantrell es un síndrome sumamente raro en el cual se asocia ectopia cordis y alteraciones de la línea media. Presentamos el caso de un paciente con pentalogía de Cantrell con ectopia cordis completa sin anomalías intracardiacas ...
Miguel A. Medina-Andrade +6 more
doaj +1 more source
Untreated patient of Pentalogy of Cantrell surviving into the sixth decade: A unique case report
Pentalogy of Cantrell is a rare syndrome consisting of a constellation of congenital anomalies including omphalocoele, lower sternal defect, sdiaphragmatic defect, diaphragmatic pericardial defect and congenital heart disease.
Neha Nischal +3 more
doaj +1 more source
FilaminA and Formin2 regulate skeletal, muscular, and intestinal formation through mesenchymal progenitor proliferation. [PDF]
The effects of actin dependent molecular mechanisms in coordinating cellular proliferation, migration and differentiation during embryogenesis are not well-understood.
Gewei Lian +3 more
doaj +1 more source
ABSTRACT Major advances in understanding human biology and health have been made possible by long‐term field research projects with Indigenous peoples, whose ecological settings and lifeways are distinct from majority populations in high‐income settings.
J. Josh Snodgrass +7 more
wiley +1 more source
Pentalogy of Cantrell – a case report
A very rare syndrome of congenital defects, comprising an abdominal wall defect, diaphragmatic hernia, defect of the diaphragmatic part of the pericardium, heart malformations, ectopia cordis and sternal defects is known as pentalogy of Cantrell.
Iwona Klisowska +3 more
doaj +1 more source
Cantrell Syndrome: A Rare Case Report [PDF]
Cantrell syndrome is a rare syndrome of congenital defects involving the abdominal wall, sternum, diaphragm, pericardium and the heart. The spectrum of anomalies varies widely. Less than 160 cases have been described in the world literature. We reported a premature infant, with the syndrome.
YILMAZ, ERDAL +5 more
openaire +2 more sources
This meta‐analysis reveals that a significant proportion of patients with POTS experience gastrointestinal symptoms. The most prevalent symptoms include nausea, bloating, abdominal pain, and postprandial fullness. There is a notable overlap of POTS with IBS, joint hypermobility, mast cell activation syndrome, and chronic fatigue.
Dmitrii Kulin +9 more
wiley +1 more source
First report of pentalogy of Cantrell in a calf: a case report
This report describes the diagnostic evaluation in a one-week-old, female Simmental twin-calf with the anamnesis of umbilical hernia. Weakness, anaemia, tachycardia and a systolic left sided murmur were significant clinical findings.
M. Floeck +7 more
doaj +1 more source
Outcomes for Congenital Diaphragmatic Hernia in Three Decades: A Report From a UK Surgical Centre
ABSTRACT Aims Congenital diaphragmatic hernia (CDH) is associated with lung hypoplasia, pulmonary hypertension and high mortality. Three decades experience from a UK centre is reported. Methods Medical records of CDH newborns between February 1990 and November 2021 and attending a multidisciplinary clinic were examined. Survival and health outcomes are
Wan Teng Lee, Paul D. Losty
wiley +1 more source
Coincidence of Incomplete Pentalogy of Cantrell and Meningomyelocele in a Dizygotic Twin Pregnancy
Pentalogy of Cantrell is an extremely rare and lethal syndrome. Ectopia cordis is frequently found in fetuses with POC but not required for incomplete forms. Likewise, meningomyelocele is a relatively uncommon neural tube defect affecting central nervous
Hakan Timur +4 more
doaj +1 more source

