Results 61 to 70 of about 6,719 (242)

Pyloric Stenosis in Premature Twins: A Case Report

Journal of Paediatrics and Child Health, Volume 61, Issue 7, Page 1148-1151, July 2025.
S. P. Y. Tan Tanny, K. Vanhaltren, M. Ditchfield, M. Pacilli, R. M. Nataraja   +4 more
wiley   +1 more source

Recurrent pyloric stenosis and definitive operative management with repeat pyloromyotomy

Journal of Pediatric Surgery Case Reports, 2019
Laparoscopic pyloromyotomy was completed successfully at 3 weeks of life after the full term delivery of a baby boy. A 3-week-old baby boy initially presented with a typical history and physical examination for hypertrophic pyloric stenosis that was ...
John Kuckelman, Chris Marenco, Woo Do, Meade Barlow   +3 more
doaj  

Infantile hypertrophic pyloric stenosis and bilious vomiting: An unusual presentation

Journal of Clinical Sciences, 2017
Infantile hypertrophic pyloric stenosis (IHPS) is a common cause of gastric outlet obstruction in infants, presenting with nonbilious projectile vomiting.
Justina O Seyi-Olajide, Oluwaseun A Ladipo-Ajayi, Adesoji O Ademuyiwa, Olumide A Elebute, Felix M Alakaloko, Christopher O Bode   +5 more
doaj   +1 more source

Estudio retrospectivo de pacientes intervenidos de estenosis hipertrófica de píloro en el HCUV entre 2009 y 2018 [PDF]

, 2019
La estenosis hipertrófica del píloro (EHP) es la etiología más frecuente de cirugía en los lactantes menores de 6 meses, y la segunda en lactantes menores de 2 meses superada únicamente por las hernioplastias.
González Terrón, Álvaro
core  

Clinical Findings Versus Imaging Studies in the Diagnosis of Infantile Hypertrophic Pyloric Stenosis [PDF]

, 2020
Background: Infantile hypertrophic pyloric stenosis is the commonest surgical cause of vomiting in early infancy and can be diagnosed clinically or by imaging studies. OBJECTIVES: To assess the accuracy of clinical examination as compared with ultrasound
Hameed, Sirar Qahtan, Khaleel, Haider Ibraheem, mohammed, Ahmed kadhum   +2 more
core   +1 more source

Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)

American Journal of Medical Genetics Part A, Volume 194, Issue 10, October 2024.
Abstract Myhre syndrome is an increasingly diagnosed ultrarare condition caused by recurrent germline autosomal dominant de novo variants in SMAD4. Detailed multispecialty evaluations performed at the Massachusetts General Hospital (MGH) Myhre Syndrome Clinic (2016–2023) and by collaborating specialists have facilitated deep phenotyping, genotyping and
Angela E. Lin, Eleanor R. Scimone, Robyn P. Thom, Duraisamy Balaguru, T. Bernard Kinane, Peter P. Moschovis, Michael S. Cohen, Weizhen Tan, Cole D. Hague, Katelyn Dannheim, Lynne L. Levitsky, Evelyn Lilly, Daniel V. DiGiacomo, Kara M. Masse, Sarah M. Kadzielski, Claire A. Zar‐Kessler, Leo C. Ginns, Ann M. Neumeyer, Mary K. Colvin, Jack S. Elder, Christopher P. Learn, Hongmei Mou, Kathryn M. Weagle, Karen A. Buch, William E. Butler, Kenda Alhadid, Patricia L. Musolino, Sadia Sultana, Dhrubajyoti Bandyopadhyay, Otto Rapalino, Zachary S. Peacock, Elizabeth L. Chou, Gena Heidary, Aaron T. Dorfman, Shaine A. Morris, James D. Bergin, Jonathan H. Rayment, Lisa A. Schimmenti, Mark E. Lindsay, MGH Myhre Syndrome Study Group, Luisa Paredes Acosta, Jennifer A. Bassetti, Sarah Bowdin, Joy A. Bress, Joseph A. Camarda, Joanne S. Chiu, C. Eduardo Corrales, Gregory Costain, Mary Beth P. Dinulos, Rajiv Devanagondi, Emily S. Doherty, John Dykes, Ann‐Christine Duhaime, Robert F. English, Elizabeth Fieg, Nora D. B. Friedman, Carl P. Garabedian, Samantha Glowacki, Barbara R. Gottlieb, Mary Hope Griffin, Frances J. Hayes, Stephanie R. Hicks, Alicia M. Hinze, Brigette A. Jason, Joel Krier, Kristen Lindgren, Michael Lyons, Adnan Majid, Hannah C. Mannem, Marie McDonald, Vinod Misra, Amy Morgan, Barbara J. Nath, Michele Ploutz, Eloise J. Prijoles, Margaret B. Pulsifer, Alicia M. Quesnel, Farrah Rajabi, Mersedeh Rohanizadegan, Ana Maria Rosales, Holly Rothermel, Edith Schussler, Elizabeth A. Sellars, Joseph Shieh, Stephanie Sherrill, Heidi Taska‐Tench, Matthew Thompson, George E. Tiller, Stephanie E. Vallee, David Viskochil, Stephanie Ware, Rachel C. Whooten, Samuel Yang, Elaine H. Zackai, Dala Zakaria   +94 more
wiley   +1 more source

Learning curves for pediatric laparoscopy: how many operations are enough? The Amsterdam experience with laparoscopic pyloromyotomy [PDF]

, 2010
Few studies on the surgical outcomes of open (OP) versus laparoscopic pyloromyotomy (LP) in the treatment of hypertrophic pyloric stenosis have been published.
C Ramstedt, E Sitsen, EC Downey Jr, GA Grant, H. A. Heij, JL Alain, KC Tan, KL Greason, KV Everett, L. T. Hoekstra, M. W. N. Oomen, MD Leclair, OO Adibe, P Healey, R. Bakx, RJ Scorpio, SD St Peter, SD St Peter, SS Kim, T Fujimoto, WL Kramer   +20 more
core   +7 more sources

Late onset Infantile Hypertrophic Pyloric Stenosis

Journal of Pediatric Surgery Case Reports, 2018
Infantile Hypertrophic Pyloric Stenosis (IHPS) is one of the most common surgical conditions of the newborn. It occurs at a rate of 1–4 per 1000 live births. Males are affected more often with a 4:1 male-to-female ratio.
Ali F. Al-Mayoof, Ibraheem K. Doghan
doaj   +1 more source

A double-masked placebo-controlled trial of azithromycin to prevent child mortality in Burkina Faso, West Africa: Community Health with Azithromycin Trial (CHAT) study protocol. [PDF]

, 2019
BACKGROUND:Biannual, mass azithromycin distribution has previously been shown to reduce all-cause child mortality in sub-Saharan Africa. Subgroup analysis suggested that the strongest effects were in the youngest children, leading to the hypothesis that ...
Bagagnan, Cheik, Boudo, Valentin, Bountogo, Mamadou, Brogdon, Jessica M, Bärnighausen, Till, Coulibaly, Boubacar, Doan, Thuy, Lebas, Elodie, Lietman, Thomas M, Lin, Ying, Oldenburg, Catherine E, Ouattara, Mamadou, Porco, Travis C, Sié, Ali, Étude CHAT Study Group   +14 more
core  

Antenatal diagnosis and management of fetal inguinoscrotal hernia: A case report with literature review

Journal of Clinical Ultrasound, Volume 52, Issue 8, Page 1198-1203, October 2024.
The fetus testicular descent begins from 24 to 25 weeks' gestation. Descent begins after 32 weeks of gestational age in 97% of the fetuses. Pediatric inguinoscrotal hernia is a common surgical condition, but only 21 cases of fetal inguinoscrotal hernia have been reported. It should not be overlooked in prenatal examination.
Ji‐Su Seong, Yoo‐Min Kim, Gina Nam, Gwang‐Jun Kim   +3 more
wiley   +1 more source