Results 61 to 70 of about 6,229 (210)

Neonatal Sacrococcygeal Mass: From Lipoma to Teratoma

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Sacrococcygeal masses in neonates that appear benign, such as presumed lipomas, may conceal germ cell tumors. Careful clinical evaluation, functional anorectal assessment, and magnetic resonance imaging are essential to differentiate benign lesions from sacrococcygeal teratomas and guide appropriate surgical management and follow‐up.
Delia Argüelles Balas, Rosa María Zubimendi Pérez, Carolina González González, Rafael Arroyo Crespo, Juan López Carnero   +4 more
wiley   +1 more source

Isolated giant intrathoracic meningocele associated with vertebral corpus deformity

, 2004
Published reports of intrathoracic meningocele with vertebral corpus defects in the absence of neurofibromatosis are very rare. We report a 9-year-old male with intrathoracic meningocele.
Turgut M., Topcuoglu M.S., Cihangiroglu M., Alhan C.   +3 more
core   +1 more source

Meningocele torácico y lumbar asociada con neurofibromatosis tipo 1. A propósito de un caso [PDF]

, 2015
Introducción: se presentó al servicio de medicina interna del Hospital Universitario San Jorge, (Pereira), el caso de una paciente de 48 años con diagnóstico de neurofibromatosis tipo 1, con síntomas de 3 meses de disnea, dolor torácico izquierdo, tos ...
Ruiz, Víctor Hugo Ruiz, Arciniegas, William ., Ospina Ramírez, Juan José   +2 more
core   +1 more source

Meningocele sacral oculta: Relato de caso

Brazilian Neurosurgery, 2005
Os autores apresentam o caso de um paciente adulto, com sinais e sintomas de compressão de cauda eqüina, ocasionados por meningocele sacral oculta. Não havia alterações cutâneas no dorso, mas sim deformidade congênita dos pés.
Raul Starling de Barros, Tony Fabiano Gomes Santos, Jarbas Carvalhais Reis, Flavio Pinelli, Katleen Cotti Ulrich   +4 more
doaj   +1 more source

The Phenotypic and Genotypic Features of ADAMTSL4‐Related Ocular Disease

Clinical Genetics, Volume 109, Issue 4, Page 730-741, April 2026.
ADAMTSL4‐related ocular disease tends to present at a younger age and be associated with higher myopia than other forms of ectopia lentis (such as FBN1). A previously reported 20‐bp deletion (c.767_786del) was highly prevalent in this cohort (23/32), and all ectopia lentis et pupillae cases carried this variant. ABSTRACT Pathogenic variants in ADAMTSL4
Katie M. Williams, Wolfgang Berger, Samuel Koller, Fatma Kivrak Pfiffner, Alessandro Maspoli, Jiradet Gloggnitzer, Britta V. T. Brühwiler, Christina Stathopoulos, Francis Munier, Louise Allen, Christos Iosifidis, Graeme C. Black, Panagiotis I. Sergouniotis, Ian Christopher Lloyd, Christina Gerth‐Kahlert   +14 more
wiley   +1 more source

Is meningocele really an isolated lesion?

, 2001
27th Annual Congress of the International-Society-for-Pediatric-Neurosurgery -- SEP 27-30, 1999 -- SALT LAKE CITY, UTAHObject: We designed this study to elucidate the associated occult spinal lesions in patients with simple dorsal meningocele.
Ersahin, Y, Barcin, E, Mutluer, S
core   +1 more source

MENINGOCELE

Edinburgh medical journal
Citation: 'meningocele' in the IUPAC Compendium of Chemical Terminology, 5th ed.; International Union of Pure and Applied Chemistry; 2025. Online version 5.0.0, 2025. 10.1351/goldbook.10933 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
Pedro Igor de Figueiredo Turíbio, Nathalia Fran Oliveira Sousa, Vagner Brasil, Bernardo Aramuni Marian   +3 more
  +5 more sources

Bilateral Orbital Meningocele Without Frontoethmoidal Meningocephalocele: A Rare Presentation

Journal of the Dow University of Health Sciences, 2017
Introduction: Bilateral orbital meningocele is a rare congenital abnormality. In our review, no case was reported from Southeast Asia which has reported bilateral orbital meningocele with frontoethmoidal meningocephalocele.
Farheen Huda, Mariam Taufiq, Hatem Adel, Sohail Ahmed Khan, Amjad Sattar   +4 more
doaj  

Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the EUROCAT Network

Paediatric and Perinatal Epidemiology, Volume 40, Issue 3, Page 414-425, March 2026.
ABSTRACT Background Surveillance of congenital anomaly prevalence over time can identify new teratogens. Anomalies with a genetic cause are excluded from the monitoring. Objectives We examined temporal changes in the proportion of genetic diagnoses among cases with a congenital anomaly.
Jorieke E. H. Bergman, Annie Perraud, Ester Garne, Ingeborg Barisic, David Tucker, Elisa Ballardini, Lea Bruneau, Clara Cavero‐Carbonell, Ianis Cousin, Miriam Gatt, Katya Kovacheva, Anna Latos‐Bielenska, Mary O'Mahony, Isabelle Monier, Isabelle Perthus, Riccardo Pertile, Anke Rissmann, Florence Rouget, Michelle Santoro, Joanna Sichitiu, Christine Verellen‐Dumoulin, Wladimir Wertelecki, Diana Wellesley, Joan K. Morris   +23 more
wiley   +1 more source

Mortality Through 2021 Among Persons Born With Spina Bifida in Metropolitan Atlanta, 1981–2018

Birth Defects Research, Volume 118, Issue 2, February 2026.
ABSTRACT Introduction Information on prevalence, predictors, and causes of mortality is sparse among persons born with spina bifida (SB), especially adults over age 25 years. Methods Individuals with SB born in 1981–2018 were identified in surveillance data from the Metropolitan Atlanta Congenital Defects Program, an active population‐based birth ...
Vijaya Kancherla, Victoria Konrad Markwalter, Janet Cragan, Elizabeth B. Gray, Catharine Riley, Jennita Reefhuis   +5 more
wiley   +1 more source