Results 41 to 50 of about 714 (188)

Kagami–Ogata syndrome in a fetus presenting with polyhydramnios, malformations, and preterm delivery: a case report

Journal of Medical Case Reports, 2019
Background Kagami–Ogata syndrome is also known as paternal uniparental disomy 14 and related disorders and is caused by abnormal genomic imprinting in the long arm of the chromosome 14q32.2 region.
Haipeng Huang, Yukiko Mikami, Kosuke Shigematsu, Nozomi Uemura, Mamiko Shinsaka, Ayaka Iwatani, Fumihito Miyake, Kazuhiko Kabe, Yasushi Takai, Masahiro Saitoh, Kazunori Baba, Hiroyuki Seki   +11 more
doaj   +1 more source

An Epigastric Heteropagus Twin with Ruptured Giant Omphalocele

Journal of Neonatal Surgery, 2014
We present a case of heteropagus twins attached to the epigastric region. The neonate also had ruptured giant omphalocoele with most of gut and liver lying outside the abdominal cavity. Patient had uneventful surgery for separation of twins and repair of ruptured omphalocoele.
Sajid Hameed, Dar, Naeem, Liaqat, Javaid, Iqbal, Tariq, Latif, Asif, Iqbal   +4 more
openaire   +3 more sources

The Impact of Chlamydia Treatment During Pregnancy on Birth Defects in New York State

Birth Defects Research, Volume 118, Issue 1, January 2026.
ABSTRACT Background Chlamydia trachomatis (CT) diagnoses are highest among females of reproductive age. Yet, little is known about adverse infant outcomes associated with treatment for CT infections during pregnancy, including birth defects. Methods Using de‐identified matched data from the New York State (NYS) Sexually Transmitted Infection ...
Elizabeth M. Boos, Meredith Howley, Tomoko Udo, Alexa Freedman, Wilson Miranda, Charles Gonzalez, Rachel Hart‐Malloy   +6 more
wiley   +1 more source

Emergency treatment of a ruptured huge omphalocele by simple suture of its membrane [PDF]

Annals of Surgical Innovation and Research, 2012
La ruptura de un onfalocele enorme es una emergencia que amenaza la vida del recién nacido. Constituye una preocupación terapéutica en ausencia de prótesis, especialmente en los países en desarrollo. Estamos informando aquí el caso de un bebé recién nacido que manejamos en emergencia con éxito gracias a un tratamiento simple.
Akakpo-Numado, Gamedzi Komlatse, Gnassingbe, Komla, Boume, Missoki Azanledji, Sakiye, Kodjo Abossisso, Mihluedo-Agbolan, Komlan, Attipou, Komla, Tekou, Hubert   +6 more
openaire   +2 more sources

An unusual case of Foetal Gastroschisis with Limb aplasia and Extra-corporal liver [PDF]

, 2005
Gastroschisis represents a herniation of abdominal contents through a paramedian full-thickness abdominal fusion defect without involving the umbilical cord.
Hebbar, Shripad, N, Pratapkumar
core  

PPP1R12A Mutation Presenting With Congenital Jejunal Atresia and Short Stature: A Pediatric Endocrinology Case Report

Case Reports in Pediatrics, Volume 2026, Issue 1, 2026.
We report an 11‐year‐old Hispanic male with a PPP1R12A gene de novo heterozygous likely pathogenic mutation, p. (Gln13Arg) (CAG>CGG), c.38 A > G in Exon 1 (NM_002480.2), detected on whole‐exome trio sequencing during his short‐stature evaluation.
Rosita Saul, Maya David, Jordin Frasch, Pedro A. Sanchez-Lara, Bahareh M. Schweiger, Andrea Scaramuzza   +5 more
wiley   +1 more source

Formal saline versus honey as escharotic in the conservative management of major omphaloceles

Nigerian Postgraduate Medical Journal, 2018
Background: The use of honey as an escharotic agent in the conservative management of omphalocele major has not been widely explored in spite of its proven benefits in chronic wound management. We explored the use of local honey as an escharotic agent by
Christopher O Bode, Adesoji O Ademuyiwa, Olumide A Elebute   +2 more
doaj   +1 more source

Primary versus Staged Closure of Exomphalos Major: Cardiac Anomalies Do Not Affect Outcome [PDF]

, 2018
Aim: The objective of the study is to describe management of exomphalos major and investigate the effect of congenital cardiac anomalies. / Methods: A single-center retrospective review (with audit approval) was performed of neonates with exomphalos ...
Cross, KMK, Curry, JI, De Coppi, P, Eaton, SJ, Kiely, EM, Pierro, A, Rees, CM, Yates, RW   +7 more
core  

Fetal abdominal wall defects in an Australian tertiary setting: contemporary characteristics, ultrasound accuracy, and outcome

, 2021
Purpose: In this study, we aimed to comprehensively evaluate risk factors, ultrasound estimation of fetal weight, prenatal management, and pregnancy outcomes of gastroschisis and omphalocele at a metropolitan Australian hospital.
Di Filippo, D , Henry, A , Jiwane, A, Patel, J, Welsh, AW   +4 more
core   +1 more source

Vaginal Delivery in Cases of Prenatally Diagnosed Omphalocele: Feasibility and Outcomes

Prenatal Diagnosis, Volume 45, Issue 13, Page 1689-1697, December 2025.
ABSTRACT Objective This study aimed to assess outcomes of fetuses with prenatally detected omphalocele and the frequency of successful vaginal delivery in pregnancies with suspected non‐lethal omphalocele and intended active neonatal management and its impact on neonatal outcome.
H. Heinrich, D. Kunne, J. P. M. Derikx, E. van Leeuwen, I. H. Linskens, E. Pajkrt   +5 more
wiley   +1 more source