pentalogy


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pentalogy

[pen′tal·ə·jē]
(medicine)
Five symptoms or defects which together characterize a disease or syndrome.
References in periodicals archive ?
Pentalogy of Cantrell is congenital disorder which is a rare event and usuallycomprises combination of birth defects.
Embryology, sternal clefts, ectopia cordis, and Cantrell's pentalogy. Semin Pediatr Surg 2008 Aug;17(3):154-160.
Virsaviya Borun suffers from Pentalogy of Cantrell, which affects five in a million people.
The thoracoabdominal type is regarded as distinct syndrome known as pentalogy of Cantrell.
(3) Pentalogy of Cantrell: midline supraumbilical abdominal wall defect, defect of the lower sternum, defect of the diaphragmatic pericardium, deficiency of the anterior diaphragm, and congenital cardiac anomalies.
Admittedly, the pentalogy is not completely devoid of Tomeo's usual winks and gestures toward his earlier output, and his fans will also identify "reiterations" from the author's previous works.
trisomy 18, 13 and 21 in 12 (7.79%) patients, pentalogy of Cantrell in 7 (4.54%) and OEIS complex in 4 (2.59%) (Fig.
Emma's daughter, Milly, was born with a very rare condition called Pentalogy of Cantrell - a condition characterised by a combination of defects involving the diaphragm, abdominal wall, pericardium (the thin membrane that lines the heart), lower sternum and the heart.
(78) Geist argues that following the copyright pentalogy, "[t]he core of fair dealing is fairness--fairness to the copyright owner in setting limits on the use of their work without permission and fairness to users to ensure that fair dealing rights can be exercised without unnecessarily restrictive limitations".
Tetralogy of fallot and atrial septal defects are the most common cardiac anomalies associated with exomphalos.[sup][3],[5] Some syndromes associated with exomphalos are nonchromosomal disorders such as Beckwith–Wiedemann syndrome, pentalogy of Cantrell, Charge syndrome, Marshall–Smith syndrome, Goltz syndrome, fetal valproate syndrome, and chromosomal genetic disorders such as trisomies 13, 14, 15, 18, or 21.[sup][6],[7]