Results 21 to 30 of about 10,609 (274)

Geographic clusters of congenital anomalies in Argentina [PDF]

, 2016
Geographical clusters are defined as the occurrence of an unusual number of cases higher than expected in a given geographical area in a certain period of time.
Barbero, Pablo, Bidondo, Maria Paz, Gili, Juan Antonio, Gimenez, Lucas Gabriel, Groisman, Boris, Liascovich, Rosa, López Camelo, Jorge Santiago, Poletta, Fernando Adrián   +7 more
core   +1 more source

Prenatal diagnosis of fetal omphalocele by ultrasound: A comparison of two centuries

Taiwanese Journal of Obstetrics & Gynecology, 2013
An omphalocele, a fetal abdominal defect, is a very important congenital anomaly. Prenatal diagnosis of fetal omphalocele is crucial to clinical management.
Yu-Ling Liang, Lin Kang, Pei-Ying Tsai, Yueh-Chin Cheng, Huei-Chen Ko, Chiung-Hsin Chang, Fong-Ming Chang   +6 more
doaj   +1 more source

Management of giant omphalocele with intestinal perforation

Journal of Pediatric Surgery Case Reports, 2021
Case of a male infant delivered at 36 weeks of gestational age and found to have a giant omphalocele, later complicated by intestinal perforation. A giant omphalocele is an omphalocele with an opening greater than 5 cm in diameter and containing the ...
Ritah Chumdermpadetsuk, Sandra Kabagambe, Vincent Duron   +2 more
doaj   +1 more source

A case of traumatic rupture of a giant omphalocele and liver injury associated with transverse lie and preterm labor

Journal of Pediatric Surgery Case Reports, 2016
Perinatal omphalocele rupture is a rare occurrence. We present a case of a baby delivered at 35 weeks with a known giant omphalocele, transverse lie, and the omphalocele downward in the birth canal who suffered rupture of the omphalocele and liver injury
Maria E. Linnaus, Britton Donato, Lisa McMahon, Linda Chambliss, David M. Notrica   +4 more
doaj   +1 more source

Omphalocele with Dextrocardia - A Rare Association

Journal of Nepal Medical Association, 2009
Omphalocele is frequently associated with many other congenital malformations. In cardiac anomalies, association of omphalocele with dextrocardia has been rarely noticed before.
Vikal Chandra Shakya, C S Agrawal, N R Shrestha, K Dhungel, S Adhikary   +4 more
doaj   +1 more source

Epigastric heteropagus and omphalocele [PDF]

Journal of Surgical Case Reports, 2020
Abstract We report a case of epigastric heteropagus twins with omphalocele. The parasite had two lower limbs, genitalia with developed phallus and scrotum but absent testis and absent anus. An omphalocele was present just below the attachment of the parasitic twin.
Mohammad Saeed Falyoun, Qusai Mashlah, Qusai Aldiri, Ali Ramadan Mohamad, Lina Khalil Daowd, Malek Ayash   +5 more
openaire   +2 more sources

Syndromes and Disorders Associated with Omphalocele (III): Single Gene Disorders, Neural Tube Defects, Diaphragmatic Defects and Others

Taiwanese Journal of Obstetrics & Gynecology, 2007
Omphalocele can be associated with single gene disorders, neural tube defects, diaphragmatic defects, fetal valproate syndrome, and syndromes of unknown etiology.
Chih-Ping Chen
doaj   +1 more source

Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele in China: a single tertiary center study

BMC Pregnancy and Childbirth, 2023
Background Patients with omphalocele, a midline abdominal wall defect at the umbilical cord base, have a low survival rate. However, the long-term outcomes of fetuses with prenatally diagnosed omphalocele have scarcely been studied.
Yanting Que, Meiying Cai, Fang Yang, Qingqiang Ji, Shuqi Zhang, Wenhui Huang, Yashi Gao, Bojing Zhou, Hailong Huang, Hua Cao, Na Lin   +10 more
doaj   +1 more source

Wandering spleen associated with omphalocele in a neonate: An unusual case with non-operative management

Journal of Pediatric Surgery Case Reports, 2017
Wandering spleen with a history of omphalocele is extremely rare. We encountered a male baby with wandering spleen associated with omphalocele. This case of wandering spleen in a neonate was diagnosed by ultrasound and computed tomography scans after ...
Daisuke Masui, Suguru Fukahori, Kimio Asagiri, Shinji Ishii, Nobuyuki Saikusa, Naoki Hashizume, Motomu Yoshida, Naruki Higasidate, Saki Sakamoto, Shiori Tsuruhisa, Yoshiaki Tanaka, Minoru Yagi   +11 more
doaj   +1 more source

Multiple Haemangiomas, Diaphragmatic Eventration and Beckwith-Wiedemann Syndrome: An Unusual Association [PDF]

, 2013
A 6-month-old girl with Beckwith-Wiedemann syndrome, multiple haemangiomas (axillary, laryngeal, pulmonary and hepatic) and diaphragmatic eventration was reported. All tumours responded to treatment with propranolol.
Borges, C, Francisco, T, Gonçalves, RM, Neto, MT   +3 more
core   +1 more source