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http://dx.doi.org/10.1093/ejcts/ezr264 | DOI Listing |
Transplant Proc
April 2025
Organ Transplant Center of Excellence, King Faisal Specialized Hospital and Research Center, Riyadh, Saudi Arabia.
Esophageal tuberculosis (TB) is a rare finding, and esophageal TB fistulas are even rarer. In general, esophageal fistulas are an uncommon finding in everyday practice, but it is frequently seen in advanced endoscopy centers. It can be either congenital or acquired.
View Article and Find Full Text PDFJ Equine Vet Sci
March 2025
Equine Veterinary Medical Center, Member of Qatar Foundation, Al Shaqab Street, Education City, Doha 00000, Qatar. Electronic address:
Tracheal congenital defects are infrequent but serious findings in animals. Tracheal diverticula are congenital air-filled cystic lesions, a sub-type of paratracheal air cyst mainly found extra-thoracically in foals. We describe a case in a twelve-day old show Arabian colt with right sided unilateral cervical swelling since birth.
View Article and Find Full Text PDFInt J Mol Sci
February 2025
Department of Pathology, George Emil Palade University of Medicine, Pharmacy, Science and Technology of Targu Mures, 540142 Targu Mures, Romania.
Congenital diaphragmatic hernia (CDH) is a relatively rare and severe developmental disease. Even with the most recent multidisciplinary therapies, the risk for neonatal mortality and morbidity remains high. Recent advancements in prenatal treatments, alongside experimental and clinical data, suggest that fetoscopic endoluminal tracheal occlusion (FETO) promotes lung development and offers a promising strategy against lung hypoplasia and pulmonary hypertension.
View Article and Find Full Text PDFPediatr Cardiol
February 2025
Division of Pediatric Cardiology, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Vascular rings are rare congenital defects that can cause tracheal and/or esophageal compression. Prenatal detection is increasing due to advances in screening and fetal echocardiography. Postnatal outcomes remain variable.
View Article and Find Full Text PDFEur J Hum Genet
February 2025
Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
We encountered two affected male patients born to non-consanguineous parents, who presented with prenatal-onset severe growth impairment, primary microcephaly, developmental delay, adrenal insufficiency, congenital glaucoma, delayed bone aging, craniosynostosis, congenital tracheal stenosis, and primary hypogonadism. By exome sequencing, we identified compound heterozygous TEDC1 variants (NM_001134877.1 c.
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