Midline defects: omphalocele, sternal cleft, diaphragmatic, pericardial and cardiac anomalies.
- Specialty
- Cardiology
- Subspecialty
- Cardiology / Congenital heart disease
- Sex & age distribution
- Male: affected, more common; Female: affected; Children: yes, neonatal
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- Cantrell syndrome
Etiology & mechanism
Early embryonic midline mesoderm defect.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (7)
In plain terms, someone with Pentalogy of Cantrell may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
1 shared
Beckwith–Wiedemann syndrome
omphalocele
1 shared
Cat eye syndrome
heart defects
1 shared
CHARGE syndrome
heart defects
1 shared
Cloacal exstrophy OEIS syndrome
omphalocele
1 shared
Congenital rubella syndrome
heart defects
1 shared
Cornelia de Lange syndrome
heart defects
1 shared
Edwards syndrome
heart defects
1 shared
Ellis–van Creveld syndrome
respiratory distress
1 shared
Emanuel syndrome
heart defects
1 shared
Fetal valproate syndrome
heart defects
Shares genes with
None.
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