Results 41 to 50 of about 30,633 (210)

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

BMC 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, Marianne H. S. Hansen, Sigbjørn Lien, Maren van Son   +3 more
doaj   +1 more source

A woman with recurrent umbilical bleeding: a case report

Journal 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, Abigail K. Wegehaupt, Majken T. Wingo   +2 more
doaj   +1 more source

Prevalence of disorders recorded in Cavalier King Charles Spaniels attending primary-care veterinary practices in England [PDF]

, 2015
Concerns have been raised over breed-related health issues in purebred dogs, but reliable prevalence estimates for disorders within specific breeds are sparse.
Brodbelt, D C, Church, D B, McGreevy, P D, O'Neill, D G, Summers, J F, Thomson, P C   +5 more
core   +3 more sources

The Intra-Umbilical Approach in Umbilical Hernia

The Eurasian Journal of Medicine, 2014
To investigate the "intra-umbilical incision", a smaller incision compared to classic incisions, in cases of umbilical hernia, and which we believe will contribute to patient satisfaction in aesthetic terms, and also the practicability of such operations.The umbilical margins of eight patients with an umbilical hernia were marked between the levels of ...
KORKUT, ERCAN, ARSLAN, ŞÜKRÜ
openaire   +3 more sources

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

Journal 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, Ria Sharma, Aryan Momin, Anirudh Shah   +3 more
doaj   +1 more source

Stratification of surgical site infection by operative factors and comparison of infection rates after hernia repair [PDF]

, 2014
OBJECTIVE: The National Healthcare Safety Network does not risk adjust surgical site infection (SSI) rates after hernia repair by operative factors. We investigated whether operative factors are associated with risk of SSI after hernia repair.
Fraser, Victoria J, Mines, Daniel, Nickel, Katelin B, Olsen, Margaret A, Wallace, Anna E, Warren, David K   +5 more
core   +2 more sources

De Novo Heterozygous ZFX Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Germline ZFX variants are associated with an X‐linked neurodevelopmental disorder, with 14 males and 16 females reported to date. We describe a 20‐year‐old female with a heterozygous ZFX frameshift variant, p.(Met666Valfs*2), identified by genome sequencing, previously reported in an affected male.
Iftekhar A. Showpnil, Allison Daley, Emily R. Sites, Shayne M. Plourde, Jesse M. Hunter, Dennis W. Bartholomew, April N. Lehman, Daniel C. Koboldt, Rolf W. Stottmann   +8 more
wiley   +1 more source

Gravid Uterus in an Umbilical Hernia

Case Reports in Obstetrics and Gynecology, 2012
Umbilical hernias large enough to contain a gravid uterus are rare. We report a case of a woman with prolapse of a gravid uterus through a previously repaired umbilical hernia.
Lawrence C. E. Mbuagbaw, Frederick L. I. Morfaw   +1 more
doaj   +1 more source

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy. [PDF]

, 2020
Developmental and epileptic encephalopathies are a heterogeneous group of early-onset epilepsy syndromes dramatically impairing neurodevelopment. Modern genomic technologies have revealed a number of monogenic origins and opened the door to therapeutic ...
Alix, E, Alkaya, DU, Ashrafzadeh, F, Becker, F, Bilguvar, K, Chatron, N, de Bellescize, J, EuroEpinomics-RES consortium AR working group, Gunes, N, Hardies, K, Hussien, H, Karimiani, EG, Kok, F, Labalme, A, Lerche, H, Lesca, G, Maroofian, R, May, P, Morsy, H, Moslemi, A-R, Nabil, A, Najafi, M, Omar, T, Poulat, A-L, Ramos, L, Roselli, S, Sanlaville, D, Schmidts, M, Tajsharghi, H, Tuysuz, B, Weckhuysen, S   +30 more
core   +2 more sources

Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Rare diseases impact approximately 1 in 10 people worldwide, and yet, less than 5% of all rare diseases currently have an approved treatment option available. This is due to many challenges unique to rare diseases, including small, diverse patient populations, the cost of drug development that is not proportionate to the number of patients who
Caleb P. Bupp, Elizabeth A. VanSickle, Julianne Michael, Chad R. Schultz, Kelly Nguyen, Melissa Hoefer, Surender Rajasekaran, André S. Bachmann   +7 more
wiley   +1 more source