نتایج جستجو برای: congenital diaphragmatic hernia

تعداد نتایج: 143969  

Journal: :Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2014
Uzma Saeed Naveed Mazhar Shahla Zameer

Congenital diaphragmatic hernia is a very common intrathoracic fetal anomaly with Morgagni hernia typically seen on right side anteriorly and Bochdalek hernia on left side posteriorly, because of the protective effects of liver and heart on either side respectively. Hiatal hernias range from herniation of a small portion of stomach into thoracic cavity to herniation of entire stomach into the l...

2015
Vishnu Bhat

Hiatal Hernia is rarely seen in a neonate. The mode of presentation in the neonatal period can be confused with the possibility of a congenital diaphragmatic hernia and other chest pathologies. The upper gastrointestinal tract contrast study is diagnostic in this disease, but careful viewing of the plain X-ray of the chest can also suggest the diagnosis.

2017
Tushar Patial Sunil Negi Vikrant Thakur

Congenital diaphragmatic hernias are infrequently encountered in adult patients. A rare type of this hernia is the Morgagni's hernia. Although they remain asymptomatic in a majority of patients, we present the case of an elderly patient who presented to us with abdominal pain and upper gastrointestinal bleeding.

2016
Thomas Bogs Florian Kipfmüller Nicolai Kohlschmidt Ulrich Gembruch Andreas Müller Heiko Reutter

BACKGROUND Previous reports of chromosomal aberrations in different forms of congenital diaphragmatic hernia have been described as comprising aneuploidies (for example, trisomy 21), microdeletions, and duplications (for example, monosomy 15q24, 22q11.2). CASE PRESENTATION We describe the first association of a de novo partial tetrasomy 4q35.2 in a father with left-sided, isolated renal agene...

2013
Bilal Mirza

Anorectal malformations (ARM) are associated with a myriad of congenital anomalies. The prevalence rates of associated anomalies range from 20% to 80%, commonest being urogenital anomalies. Other important associations and syndromes include Down syndrome and VACTERL (vertebral, anorectal, cardiac, trachea-esophageal, renal, limb) anomalies [1]. ARM has rarely been described in association with ...

2011
Prince Raj Yogesh Kumar Sarin

Morgagnis hernia is rare in pediatrics, representing 1%-6% of all congenital diaphragmatic hernias (CDH). We report a young boy presented with obstructive jaundice caused by compression of common bile duct (CBD) due to stretching and rotation of second part of duodenum in right-sided Morgagni hernia. Such presentation is rarely reported in literature.

حقیقی, لادن,

The field of prenatal diagnosis of congenital anomalies has had great advances in recent years. Today we are able to diagnose different fetal anomalies in early developmental stages, and correct some of them, through prenatal fetal surgery. In this paper, we begin by describing the advances in surgical treatment of some fetal diseases such as, diaphragmatic hernia, lung sequestration, pleural e...

Journal: :Endoscopy 2008
B Bigler T Steffen J Binek

for decompression colonoscopy having been admitted 2 days previously for bow− el obstruction. Upon admission, the patient had slight abdominal distension. Analgesic and laxative treatments were initiated but proved ineffective, and conventional radiography showed increasing disten− sion of the cecum. Colonoscopy was per− formed up to the left colonic flexure (l" Fig. 1 a), and radiographic cont...

Journal: :Pediatrics 2004
Coranne D Tesselaar Roelf R Postema Marieke F van Dooren Karel Allegaert Dick Tibboel

Congenital diaphragmatic hernia is a relatively rare disorder (1:3000 newborns) that frequently presents with respiratory distress in the immediate neonatal period due to severe pulmonary hypertension and lung hypoplasia. Extracorporeal membrane oxygenation (ECMO) can be used as a last resort when artificial ventilation and/or modulation of the pulmonary vascular tone fail to improve the clinic...

2017
Nives Zimmermann Jerzy Stanek

BACKGROUND Simpson-Golabi-Behmel syndrome (SGBS) is a rare X-linked recessive syndrome characterized by fetal overgrowth. CASE REPORT We present a case of a male infant with SGBS. Abnormal prenatal ultrasound (including congenital diaphragmatic hernia) prompted microarray testing of amniotic fluid cells, which showed deletion on chromosome Xq26.2 affecting the glypican-3 gene consistent with SG...

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