Results 121 to 130 of about 57,963 (216)

Surgical correction of a double congenital hernia in a veal calf

Veterinary Record Case Reports, Volume 14, Issue 2, May 2026.
Abstract This clinical case report describes the rare occurrence and successful surgical management of two simultaneous congenital hernias, umbilical and perineal, in a crossbred veal calf. At 5 days of age, the animal, weighing approximately 40 kg, showed visible swelling in the umbilical and perineal regions together with a congenital tail ...
Andrea Spadaro, Veronica Cristina Neve, Giovanna Lucrezia Costa, Roberto Puleio, Filippo Spadola   +4 more
wiley   +1 more source

Children With Biliary Atresia Have Substantial Morbidity in Early Childhood and a High Risk of Liver Transplantation. [PDF]

Birth Defects Res
Damkjær M, Tan J, Loane M, Given J, Ballardini E, Cavero-Carbonell C, Gissler M, Jordan S, Pierini A, Rissmann A, Tucker D, Garne E, Morris JK.   +12 more
europepmc   +1 more source

Histological Characterization and Oocyte Development in Pearlspot, Etroplus suratensis (Bloch, 1790) From Vembanad Lake, Kerala, India

Aquaculture, Fish and Fisheries, Volume 6, Issue 2, April 2026.
ABSTRACT This study is the first to elucidate the oocyte growth pattern of Etroplus suratensis through detailed gonad histology. Ovary samples from different maturity stages were collected from October 2023 to September 2024 from cage culture systems installed in Vembanad Lake, Kumbalangi, Kerala, India.
Mohammad Saddam Hussain, Mahadevan Harikrishnan, Dinesh Yadav, Betsee Thomas, Keerthana PV, Nikhila Khanna AR, Haritha Haridas, Mohamad Husneid Azad, Akhil Soman   +8 more
wiley   +1 more source

Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea

American Journal of Medical Genetics Part A, Volume 200, Issue 4, Page 937-946, April 2026.
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat, Marjolaine Champagne, Mathieu Bergeron, Philippe Dodin, Nadia Roumeliotis   +4 more
wiley   +1 more source

Adult presentation of unilateral pulmonary venous atresia: CT findings in a rare congenital anomaly. [PDF]

Radiol Case Rep
Ricardo JC, Saavedra S, Pinto AD, Prada MA, Mejía AF, Martínez V, Rivera AL.   +6 more
europepmc   +1 more source

Variants in AKR1D1 and Infant Mortality: Should Bile Acid Screening be a Routine Part of Newborn Screening?

American Journal of Medical Genetics Part A, Volume 200, Issue 4, Page 971-977, April 2026.
ABSTRACT Biallelic pathogenic variants in AKR1D1 cause Δ4‐3‐oxosteroid 5β‐reductase deficiency, disrupt bile acid synthesis, and result in Congenital Bile Acid Synthesis defect type 2 (CBAS2). CBAS2 presents in infancy with cholestasis, coagulopathy, and failure to thrive.
Jade Hudson, Stephanie Hyunh, Bojana Rakic, Cornelius Boerkoel   +3 more
wiley   +1 more source

PPP1R12A Mutation Presenting With Congenital Jejunal Atresia and Short Stature: A Pediatric Endocrinology Case Report. [PDF]

Case Rep Pediatr
Saul R, David M, Frasch J, Sanchez-Lara PA, Schweiger BM.   +4 more
europepmc   +1 more source

Clinical outcomes after nondiagnostic prenatal exome sequencing: Need for balancing reassurance and residual risks in genetic counseling

Journal of Genetic Counseling, Volume 35, Issue 2, April 2026.
Abstract The clinical application of prenatal exome sequencing (pES) for fetal structural anomalies is relatively new. Although a prenatal genetic diagnosis has been shown to have high clinical and personal utility for families, nearly 70% of pregnancies undergoing pES will receive nondiagnostic results.
Sophie Albert, Anne Swenerton, Kirsten M. Niles, Sylvie Langlois, Jessica L. Zambonin   +4 more
wiley   +1 more source

Fetal MRI: abdominal cystic lesions. [PDF]

Insights Imaging
Castellanos DG, Rodríguez MR, Greciano LS, Del Hoyo AA, Moreno AD, Alcolea JL, Sampietro C, de Vega VM.   +7 more
europepmc   +1 more source

Inflammatory Markers Stratify Surgical Outcomes in Pediatric Airway Reconstruction

The Laryngoscope, Volume 136, Issue 4, Page 1920-1927, April 2026.
ABSTRACT Objectives Red blood cell distribution width (RDW) predicts surgical success in adult patients undergoing open airway reconstruction for laryngotracheal stenosis, but similar biomarkers in pediatrics remain unidentified. This study identifies predictors of outcomes in pediatric patients undergoing triple endoscopy or surgical airway ...
Nomongo Dorjsuren, Hrithik Praveen, Kalpnaben Patel, Shilin Zhao, Alexander Gelbard, Christopher Wootten   +5 more
wiley   +1 more source