Results 161 to 170 of about 33,846 (262)

Conservative Management Enabling Spontaneous Passage of an Idiopathic Primary Spontaneous Enterolith: A Case Report and Literature Review

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Enterolithiasis—formation of stone concretions within the gastrointestinal tract—is an uncommon and underrecognized cause of intermittent abdominal symptoms and acute bowel obstruction. Primary (true) enteroliths originate within the bowel lumen and are usually associated with focal stasis from anatomic or inflammatory pathology; idiopathic ...
Lensa Million Baharu, Ragasa Getachew Bayisa, Zenebe Teklu Gebremariam, Esmael Mohamed Dawud, Nigusu Solomon Herego, Nahom Teklu Maru, Webi Alemayehu Tulu, Ahmedin Solomon Kedir, Tamirat Godebo Woyimo   +8 more
wiley   +1 more source

Acute Intestinal Obstruction Revealing an Internal Hernia of the Broad Ligament Following Promontofixation: A Case Report. [PDF]

Cureus
Mohamed L, Mougib H, Madani AM, Ouazni M, Soufi M.   +4 more
europepmc   +1 more source

Nonlinear Association Between the C‐Reactive Protein‐To‐Albumin Ratio and Post‐Stroke Epilepsy Risk

CNS Neuroscience &Therapeutics, Volume 32, Issue 7, July 2026.
The C‐reactive protein‐to‐albumin ratio (CAR) is a robust, independent predictor of post‐stroke epilepsy (PSE) in ischemic stroke patients, exhibiting a nonlinear, threshold‐dependent association. As an integrative biomarker, CAR holds promise for enhancing early risk stratification and informing personalized intervention strategies.
Xiao Wu, Yingru Zhou, Qi Yang, Yunliang Tang   +3 more
wiley   +1 more source

Internal Hernia: A Rare Cause of Bowel Ischemia and Infarction. [PDF]

Cureus
Bairwa BL, Manjra S, Gupta S.
europepmc   +1 more source

Neonatal developmental and epileptic encephalopathy with movement disorder and arthrogryposis: A shared phenotype across brain‐expressed sodium channelopathies

Epilepsia, Volume 67, Issue 7, Page 3629-3643, July 2026.
Abstract Objective Neonatal developmental and epileptic encephalopathy with movement disorder and arthrogryposis (NDEEMA) represents the most severe end of the gain‐of‐function (GOF) SCN1A disorder spectrum. Sporadic cases of congenital arthrogryposis have also been reported in individuals with SCN2A‐, SCN3A‐, and SCN8A‐related developmental and ...
Sopio Gverdtsiteli, Sebastian Ortiz, Tobias Brünger, Francesca Furia, Carmen Barba, Trine Bjørg‐Hammer, Ingo Borggraefe, Roberto Caraballo, Sebahattin Cirak, Alberto Espeche, Walid Fazeli, Renzo Guerrini, Matias Juanes, Karin Kassahn, Maria Kinali, Johannes Krämer, Judith Kröll, Maria Concepción Miranda Herrero, Renske Oegema, Katrin Ounap, Oscar Peñuela, Konrad Platzer, Asuri Narayan Prasad, Aurora Pujol, Karit Reinson, Alfonso Represa, Eugenia Roza, Gabriela Reyes Valenzuela, Agustí Rodríguez‐Palmero, Suzanne Sallevelt, Maria Iciar Sanchez‐Albiusa, Ingrid E. Scheffer, Cory Smid, Carl E. Stafstrom, Eva‐Lena Stattin, Jen R. Suarez, Steffen Syrbe, Kette D. Valente, Matias Wagner, Saskia Wortmann, Elena Gardella, Dennis Lal, Andreas Brunklaus, Rikke S. Møller   +43 more
wiley   +1 more source

Internal hernia through an idiopathic transverse mesocolon defect treated by laparoscopic surgery: a case report. [PDF]

Int J Surg Case Rep
Inoue D, Tokuhara K, Matsuki H, Noda R, Kataoka N.   +4 more
europepmc   +1 more source

Clinical and Genetic Spectrum of Filippi Syndrome: A Systematic Review of Published Case Reports and Case Series

Health Science Reports, Volume 9, Issue 7, July 2026.
ABSTRACT Background and Aims Filippi syndrome is a very rare autosomal recessive craniodigital disorder primarily caused by mutations in the gene CKAP2L, characterized by syndactyly, microcephaly, growth retardation, distinctive craniofacial features, and intellectual disability.
Muhammad Anas Faheem, Laraib Ghanghro, Ayesha Khan, Maryam Khalid, Salwa Bashir, Dania Iqbal, Adan Ali, Hussain Haider Shah, Sameer Abdul Rauf, Humaira Kalam   +9 more
wiley   +1 more source

A Case of Pediatric Internal Hernia Heralded by Constipation. [PDF]

Cureus
Adams CP, Meyers LY, Rodriguez RJ, Neil HO, Oliver JJ.   +4 more
europepmc   +1 more source

Long‐Term Follow‐Up of Patients With Mitochondrial Carbonic Anhydrase VA Deficiency. A Case Report and Literature Review

JIMD Reports, Volume 67, Issue 4, July 2026.
ABSTRACT Mitochondrial carbonic anhydrase VA (CA‐VA) deficiency is a rare inherited metabolic disorder caused by biallelic variants of the CA5A gene. It presents with hyperammonemia, lactic acidosis, and ketonuria, with or without hypoglycemia. We report the long‐term follow‐up of the first two reported cases of CA‐VA deficiency: a 16‐year‐old female ...
Shaymaa Shurrab, Amira Mobarak, Gabriella Horvath, Sylvia Stocker‐Ipsiroglu, Clara van Karnebeek, Ramona Salvarinova‐Zivkovic   +5 more
wiley   +1 more source

Internal Hernia Through a Mesenteric Defect Presenting As Midgut Volvulus: A Rare and Intriguing Coexistence. [PDF]

Cureus
Shrivastava A, Karn S, Reddy A, Singh K, Kumar N.   +4 more
europepmc   +1 more source