Results 71 to 80 of about 64,532 (311)

SURGICAL TREATMENT STRATEGIES FOR GIANT ANTERIOR ABDOMINAL WALL HERNIAS

Паёми Сино, 2021
Objective: To improve surgical treatment of giant hernias of the anterior abdominal wall (AAW). Methods: For 152 patients with giant hernias of the AAW, various hernioplasty options were selected. Primary hernias occurred in 56 (36.8%), postoperative –
M.KH. MALIKOV, F.B. BOKIEV, O. M. KHUDOYDODOV, I.T. KHOMIDOV, F.M. KHOMIDOV, N.A. MAKHMADKULOVA   +5 more
doaj   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Cost-effectiveness of alternative methods of surgical repair of inguinal hernia [PDF]

, 2004
Objectives: To assess the relative cost-effectiveness of laparoscopic methods of inguinal hernia repair compared with open flat mesh and open non-mesh repair.
Aitola, P., Anderberg, B., Arvidsson, D., Barkun, J., Bay-Nielsen, M., Beets, G., Bittner, R., Bringman, S., Castoro, C., et al., Fingerhut, A., Go, P., Grant, A., Kingsnorth, A., McCormack, K., Merello, J., O'Dwyer, P., Payne, J., Ross, S., Scott, N., Vale, L.   +20 more
core   +2 more sources

Combined Long‐Read Genome and Transcriptome Sequencing Establishes Novel Variants in MEGF8 as the Cause for Carpenter Syndrome Type 2

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Carpenter syndrome type 2 (CRPT2) is a rare autosomal recessive disease mainly characterized by craniosynostosis and polysyndactyly. CRPT2 is the rarer subtype of Carpenter syndrome (CRPTS) and is caused by biallelic variants in the multiple epidermal growth factor‐like domains 8 gene (MEGF8).
Kiana Rashidi, Bhavi P. Modi, Phillip A. Richmond, Massimo Mangino, Loryn Byres, Cassie McDonald, Joshua Dalmann, Simran Samra, Kate L. Del Bel, Anna Lehman, Jessica L. Zambonin, Stuart E. Turvey   +11 more
wiley   +1 more source

Retrospective analysis of inguinofemoral hernias

Medicine Science, 2020
We aim to present the operative findings of inguinal and femoral hernias that were operated.The records of 732 patients who underwent surgery for inguinal and femoral hernia between March 2000 and January 2013 were evaluated retrospectively.
Turgay Karatas, Davut Ozbag, Murat Kanlioz   +2 more
doaj   +1 more source

Morphology of the Esophageal Hiatus: Is It Different in 3 Types of Hiatus Hernias? [PDF]

, 2020
Background/aimsThe esophageal hiatus is formed by the right crus of the diaphragm in the majority of subjects. Contraction of the hiatus exerts a sphincter-like action on the lower esophageal sphincter (LES). The aim is to study the hiatal anatomy (using
Ghahremani, Gary, Horgan, Santiago, Kumar, Dushyant, Kunkel, David C, Mittal, Ravinder K, Zifan, Ali   +5 more
core   +1 more source

Update of Guidelines for laparoscopic treatment of ventral and incisional abdominal wall hernias (International Endohernia Society (IEHS)) : Part B [PDF]

, 2019
In 2014 the International Endohernia Society (IEHS) published the first international "Guidelines for laparoscopic treatment of ventral and incisional abdominal wall hernias".
Bain, K., Bansal, V. K., Berrevoet, Frederik, Bingener-Casey, J., Bittner, R., Chen, D., Chen, J., Chowbey, P., de Beaux, A., Dietz, U. A., Ferzli, G., Fortelny, R., Hoffmann, H., Iskander, M., Jorgensen, L. N., Khullar, R., Kirchhoff, P., Koeckerling, F., Kukleta, J., LeBlanc, K., Li, J., Li, Z., Lomanto, D., Mayer, F., Meytes, V, Misra, M., Morales-Conde, S., Niebuhr, H., Radvinsky, D., Ramshaw, B., Ranev, D., Reinpold, W., Schrittwieser, R., Sharma, A., Stechemesser, B., Sutedja, B., Tang, J., Warren, J., Weyhe, D., Wiegering, A., Woeste, G., Yao, Q.   +41 more
core   +4 more sources

Expanding the Phenotype of TUFM‐Related Combined Oxidative Phosphorylation Deficiency 4

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Combined oxidative phosphorylation deficiency 4 (COXPD4) is a rare mitochondrial condition caused by biallelic deleterious variants in the nuclear‐encoded gene TUFM. To date, most individuals with COXPD4 have presented with encephalopathy, hypotonia, and abnormal brain imaging. Many of the reported individuals died in infancy. We aim to expand
Noémie Villeneuve‐Cloutier, Jodi Warman‐Chardon, Danielle K. Bourque   +2 more
wiley   +1 more source

CT diagnosis of small bowel obstruction caused by internal hernia from persistent attachment of a Meckel's diverticulum to the umbilicus by the obliterated omphalomesenteric duct [PDF]

, 2015
We report a case of small bowel obstruction (SBO) caused by internal hernia from persistent attachment of a Meckel's diverticulum (MD) to the umbilicus by the obliterated omphalomesenteric duct that was diagnosed by multidetector CT and confirmed during ...
BELLINI, DAVIDE, Cavallaro, G, De Santis, D, IORIO, OLGA, LAGHI, ANDREA, MACERONI, MARCO MARIA, Rengo, M, SILECCHIA, Gianfranco   +7 more
core   +1 more source

Genomic Contributors to Congenital Diaphragmatic Hernia: Results of Exome Sequencing in 560 Probands and Cross Reference of Findings in an Independent Cohort

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT There is a strong genetic contribution to the etiology of congenital diaphragmatic hernia (CDH). This study evaluated genetic testing results and diagnostic yield for fetuses and children with CDH. This was a retrospective cohort study of exome sequencing (ES) performed at GeneDx for fetuses and children ≤ 18 years of age with CDH compared ...
Justin Blair, Kevin Carratu, Natalie E. Rintoul, Holly L. Hedrick, William H. Peranteau, Catherine M. Avitabile, Kirsty McWalter, Paul Kruszka, Ian D. Krantz, K. Taylor Wild   +9 more
wiley   +1 more source