Results 41 to 50 of about 18,943 (222)

Spontaneous Evisceration following Ruptured Umbilical Hernia Abscess in an Infant: A Rare Case Report

open access: yesJournal of Indian Association of Pediatric Surgeons
Umbilical hernia is one of the most common congenital anomalies. We document an unusual event of abscess of umbilical hernia in a 5-month-old female which was associated with rupture of the hernia followed by evisceration.
Greeshma Suresh   +4 more
doaj   +1 more source

Case Report: 21 Cases of Umbilical Hernia Repair Using a Laparoscopic Cephalic Approach Plus a Posterior Sheath and Extraperitoneal Approach

open access: yesFrontiers in Surgery, 2021
Purpose: In this study, a novel surgical technique was developed for umbilical hernias, in which a laparoscopic cephalic approach plus a posterior sheath and an extraperitoneal approach was employed.
Kunjie Zhang, Mingfang Qin, Guoqian Ding
doaj   +1 more source

STRANGULATED UMBILICAL HERNIA [PDF]

open access: yesThe Lancet, 1875
n ...
openaire   +1 more source

Obstructed Umbilical Hernia with Cecal Perforation and Omphalitis: A Unique Case in an Infant

open access: yesJournal of Indian Association of Pediatric Surgeons
Umbilical hernia is very commonly encountered in infants. Obstruction in an umbilical hernia, though rare, has been reported in literature. We report a rare case of a 2-month-old boy who had an obstructed cecum in the umbilical hernia with localized ...
Amar Shah   +3 more
doaj   +1 more source

Genome-wide association study reveals a QTL and strong candidate genes for umbilical hernia in pigs on SSC14

open access: yesBMC Genomics, 2018
Background Umbilical hernia is one of the most prevalent congenital defect in pigs, causing economic losses and substantial animal welfare problems. Identification and implementation of genomic regions controlling umbilical hernia in breeding is of great
Eli Grindflek   +3 more
doaj   +1 more source

A woman with recurrent umbilical bleeding: a case report

open access: yesJournal of Medical Case Reports, 2022
Background Umbilical discharge in an adult is rare and generates broad diagnostic considerations. Umbilical anatomy is variable owing to congenital abnormalities and acquired pathology such as umbilical hernias.
Yong-hun Kim   +2 more
doaj   +1 more source

The Critical Role of Fractionated Urine Glycosaminoglycans in the Evaluation of Mucopolysaccharidosis Type II in Four Unrelated Families

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Since 2015, Ann and Robert H. Lurie Children's Hospital has performed diagnostic testing for infants who screen positive for mucopolysaccharidosis type II (MPS II) on the Illinois newborn screen. Preliminary diagnostic testing includes measurement of plasma iduronate‐2‐sulfatase enzyme activity and urinary glycosaminoglycan analysis, followed ...
Carly A. Rasmussen   +5 more
wiley   +1 more source

De Novo Complex Genomic Rearrangement Spanning 2q31.1 in a Proband With Congenital Malformations: Genotype–Phenotype Correlation and Development of a CGR Detection Pipeline

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The 2q31 region is commonly associated with pathogenic alleles of the HOXD cluster leading to various clinical phenotypes related to skeletal development. We present a proband with tetralogy of Fallot and multiple congenital anomalies. Genomic variant screening including an in‐house CGR detection pipeline pairing genome sequencing (GS ...
Katherine Helle   +10 more
wiley   +1 more source

Umbilical hernia: Factors indicative of recurrence

open access: yes, 2008
Umbilical hernia has gained little attention from surgeons in comparison with other types of abdominal wall hernias (inguinal, postoperative); however, the primary suture for umbilical hernia is associated with a recurrence rate of 19–54%.
Linas Venclauskas   +2 more
core   +1 more source

Long‐Term Follow Up of Two Patients With Variants in the Cluster 1031‐1159 of TRRAP Gene: Expanding the Phenotype of Developmental Delay With or Without Dysmorphic Facies and Autism

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide   +10 more
wiley   +1 more source

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