𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Antenatal diagnosis of a Morgagni hernia in the second trimester

✍ Scribed by Krishan Kumar Jain; Jyotsna Sen; Suresh Kanta Rathee; Jitender Saini


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
119 KB
Volume
36
Category
Article
ISSN
0091-2751

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Morgagni hernia is an uncommon type of congenital hernia that is rarely diagnosed antenatally. Herniation of the liver into the fluid‐filled pericardial sac resulting in a thoracic mass is a particularly rare form of Morgagni hernia; only 3 cases have been reported in the literature, all with a diagnosis made at 32 weeks' gestation or later. We report a case of Morgagni hernia diagnosed on antenatal sonography at 24 weeks' gestation. Β© 2007 Wiley Periodicals, Inc. J Clin Ultrasound, 2008


πŸ“œ SIMILAR VOLUMES


Half-Fourier acquisition single-shot tur
✍ Dean Tyrell; Feroze Mohamed; Constantinos Pavlides; Steven Kutalek; Charles Mulh πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 264 KB

## Abstract Magnetic resonance (MR) imaging with multi‐planar, gated Half‐Fourier Acquisition Single‐Shot Turbo Spin‐Echo (HASTE) imaging was performed to evaluate a woman with dysrhythmia. MR examination for right ventricular dysplasia revealed a Morgagni hernia. The HASTE images depicted well the

Sonographic diagnosis of cloverleaf skul
✍ Carl P. Weiner; Roger A. Williamson; Stephen M. Bonsib πŸ“‚ Article πŸ“… 1986 πŸ› John Wiley and Sons 🌐 English βš– 256 KB

An infant with thanatophoric dysplasia occurs in approximately 1:6,400 deliveries.' This lethal, sporadically occurring condition is readily diagnosable prenatally with ultrasound.2 The risk of recurrence is negligible since there are no documented cases involving sibs (Judith G. Hall, MD, personal

Prenatal diagnosis of thoracic kidney in
✍ Apostolos P. Athanasiadis; Menelaos Zafrakas; Christos Arnaoutoglou; Aikaterini πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 159 KB

## Abstract Ectopic kidney is a rare congenital malformation, caused by renal malpositioning during embryogenesis. We report a rare case of ectopic kidney located in the left hemithorax of a male fetus. The unique features in this case were early sonographic prenatal diagnosis of thoracic kidney at