Results 111 to 120 of about 13,044 (211)

Klippel–Trénaunay Syndrome With Pelvic/Rectal and Urinary Bladder Involvement: A Rare Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Concurrent bladder and rectosigmoid vascular malformations in Klippel–Trénaunay syndrome can mimic synchronous pelvic malignancy. Multidisciplinary clinical, radiological, endoscopic, and pathological evaluation is essential to avoid misdiagnosis and to guide appropriate, often conservative, management.
Somaya Al Kiswani, Khitam Salahat, Omar Daas, Mohammed AbdulJabbar Abed, Reem Abuhamdah, Usama Al Khuffash, Abdullah Nofal   +6 more
wiley   +1 more source

The role of age and severity of deformity in the choice of treatment for pectus carinatum: a comparison of braces and surgical correction

Journal of Cardiothoracic Surgery
Background Pectus carinatum (PC) is a congenital chest wall deformity that can lead to aesthetic, functional and psychosocial problems, especially in adolescence.
Turkan Dubus, Mehmet Ali Unal, Mehmet Yazici, Gokce Cangel, Erman Bagatur Ozturk   +4 more
doaj   +1 more source

Coexistence of Suspected Tetralogy of Fallot With Absent Pulmonary Valve and Dextrocardia in Pre‐Gestational Diabetes Mellitus: A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Early fetal echocardiography and serial surveillance are crucial in pregnancies complicated by pregestational diabetes. Tetralogy of Fallot with absent pulmonary valve syndrome may cause progressive cardiomegaly, ventricular hypertrophy, hydrops, and fetal demise.
Alireza Golbabaei, Vida Kahani, Marzieh Mousivand   +2 more
wiley   +1 more source

Mucosal‐Associated Invariant T Cells in Health and Disease

MedComm, Volume 7, Issue 10, October 2026.
The roles of MAIT cells in health and disease and their therapeutic applications. In healthy individuals, riboflavin metabolites secreted by commensal bacteria at mucosal sites are presented by MR1, leading to the activation of MAIT cells. Activated MAIT cells can maintain the barrier integrity of mucosal tissues in a steady state or migrate to the ...
Yu Zhao, Feng‐Mi Ou, Dan Liang, Yang Gao, Qing‐Qing Li, Yi‐Qun Kuang   +5 more
wiley   +1 more source

A Multidisciplinary Approach to the Anesthetic Management of Patients With Duchenne Muscular Dystrophy

Pediatric Pulmonology, Volume 61, Issue 10, October 2026.
ABSTRACT Duchenne muscular dystrophy (DMD) is an inherited neuromuscular disorder with multisystem involvement that causes progressive muscular weakness and cardiorespiratory dysfunction. The first comprehensive recommendations regarding anesthetic management are now almost 20 years old and, in the interval, DMD care has evolved.
Fabrizio Racca, Elena Conti, Giulia Racca, Luigi Barberis, David J. Birnkrant   +4 more
wiley   +1 more source

Abnormal response of costal chondrocytes to acidosis in patients with chest wall deformity. [PDF]

Exp Mol Pathol, 2019
Asmar A, Semenov I, Kelly R, Stacey M.
europepmc   +1 more source

Congenital Lung Malformations in Neonates: A 9‐Year Tunisian Cohort Highlighting Diagnostic Challenges and Outcomes in a Resource‐Limited Setting

Pediatric Pulmonology, Volume 61, Issue 10, October 2026.
ABSTRACT Background Congenital lung malformations (CLMs) represent a broad spectrum of developmental anomalies with highly variable prenatal and postnatal presentations and outcomes. Their postnatal management remains non‐standardized. This study aimed to describe the spectrum of bronchopulmonary malformations diagnosed in the neonatal period, assess ...
Hajer Chourou, Rim Ben Aziza, Wafa Belhadj Ammar, Cyrine Saadi, Maryem Marzouki, Youssef Hellal, Said Jlidi, Samia Kacem, Bilel Jerbi   +8 more
wiley   +1 more source

Use of an Optical Scanning Device to Monitor the Progress of Noninvasive Treatments for Chest Wall Deformity: A Pilot Study. [PDF]

Korean J Thorac Cardiovasc Surg, 2018
Kelly RE, Obermeyer RJ, Kuhn MA, Frantz FW, Obeid MF, Kidane N, McKenzie FD.   +6 more
europepmc   +1 more source

Mitral regurgitation and decompensated heart failure in a young pregnant pony mare: An aetiological challenge

Equine Veterinary Education, Volume 38, Issue 10, Page e676-e685, October 2026.
Summary A 4‐year‐old, 6‐month pregnant, Welsh pony mare presented with severe acute clinical signs including depression, anorexia, pale mucous membranes, tachycardia with a grade 4/6 holosystolic murmur and moderate expiratory dyspnoea with diffuse wheezes. There was no evidence of placentitis or fetal distress.
M. F. David, L. Cannon, A. Tortereau, A. Thomas‐Cancian, I. Desjardins   +4 more
wiley   +1 more source

Respiratory Physiotherapy for Chest Wall Deformity in an Infant With Neuroendocrine Cell Hyperplasia of Infancy. [PDF]

Pediatr Pulmonol
Jurkiewicz A, Marczak H, Strzelak A.
europepmc   +1 more source