Pentalogy of Cantrell: Diagnosis in the first trimester

Sarkar, Pampa; Bastin, Jean; Katoch, Daman; Pal, Arabinda

doi:10.1080/01443610500335795

Cited by 14 publications

(10 citation statements)

References 8 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Various other associated anomalies have been reported and include craniofacial and central nervous system anomalies such as cleft lip or palate, encephalocele, hydrocephalus, and craniorachischisis [12][13][14][15]; limb defects such as clubfoot, absence of tibia or radius, and hypodactyly [16,17]; and abdominal organ defects such as gall bladder agenesis and polysplenia [15].…”

Section: Discussionmentioning

confidence: 98%

Pentalogy of Cantrell: Embryofetoscopic Diagnosis

Sardo

Paladini

Zizolfi

et al. 2013

Journal of Minimally Invasive Gynecology

View full text Add to dashboard Cite

Section: Discussionmentioning

confidence: 98%

Pentalogy of Cantrell: Embryofetoscopic Diagnosis

Sardo

Paladini

Zizolfi

et al. 2013

Journal of Minimally Invasive Gynecology

View full text Add to dashboard Cite

“…Intrauterine diagnosis of this pentalogy is impossible before the 12th week of gestation, because of herniation of bowel out of abdomen is a normal event in fetal development at this time, but after that ultrasonography is a useful method even in the first trimester [ 13 ]. Both 2-dimensional ultrasonography and 3-dimensional obstetric ultrasonography are recommended, but 3D ultrasonography is not necessary in first trimester.…”

Section: Discussionmentioning

confidence: 99%

Coincidence of Incomplete Pentalogy of Cantrell and Meningomyelocele in a Dizygotic Twin Pregnancy

Tımur

Tokmak

Bayram

et al. 2015

Case Reports in Obstetrics and Gynecology

View full text Add to dashboard Cite

Pentalogy of Cantrell is an extremely rare and lethal syndrome. Ectopia cordis is frequently found in fetuses with POC but not required for incomplete forms. Likewise, meningomyelocele is a relatively uncommon neural tube defect affecting central nervous system and associated with neurological problems. Herein, we presented a woman with dizygotic twin pregnancy having coincidence of incomplete POC and MMC in each individual fetus, which has never been reported previously.

show abstract

“…Intrauterine diagnosis of PC can be easily made by US, as this method is commonly employed to examine the fetus in the first trimester. 11 , 12 The unique association of the omphalocele and EC is the hallmark of this syndrome. 13…”

Section: Discussionmentioning

confidence: 99%

Pentalogy of Cantrell: first case reported in Saudi Arabia

Bagabir

Azhar

2014

Annals of Saudi Medicine

View full text Add to dashboard Cite

Pentalogy of Cantrell (PC) is a rare congenital anomaly involving defects in the anterior diaphragm, supraumbilical abdominal wall, diaphragmatic pericardium, and lower sternum, and other congenital intracardiac abnormalities. Here, we report the case of a newborn infant who was born at 32 weeks of gestation and had all 5 features of PC, in addition to absent kidneys and a deformed left hand. Medical intervention would not be able to save the patient, so we allowed her to die in peace. We discuss here the etiology, prenatal diagnosis, and severity of and the mortality associated with this condition. To our knowledge, this was the first reported case of PC in Saudi Arabia.

show abstract

Pentalogy of Cantrell: Diagnosis in the first trimester

Cited by 14 publications

References 8 publications

Pentalogy of Cantrell: Embryofetoscopic Diagnosis

Pentalogy of Cantrell: Embryofetoscopic Diagnosis

Coincidence of Incomplete Pentalogy of Cantrell and Meningomyelocele in a Dizygotic Twin Pregnancy

Pentalogy of Cantrell: first case reported in Saudi Arabia

Contact Info

Product

Resources

About