In:
Pediatria. Journal named after G.N. Speransky, Pediatria, Ltd., Vol. 101, No. 1 ( 2022-2-18), p. 214-217
Abstract:
Pentalogy of Cantrell is a rare congenital malformation (CM), occurring with a frequency of 1:100,000 – 1:200,000 newborns, characterized by the presence of five main features: omphalocele, ectopia of the heart, absence of the lower sternum with diaphragm and pericardial defects. The description of three clinical cases of this СМ is intended to familiarize specialists with different options for tactical approach and its surgical correction.
Type of Medium:
Online Resource
ISSN:
0031-403X
,
1990-2182
Uniform Title:
КЛИНИЧЕСКИЕ НАБЛЮДЕНИЯ РЕДКОЙ ВРОЖДЕННОЙ ПАТОЛОГИИ: ПЕНТАДА КАНТРЕЛЛА (ОМФАЛОЦЕЛЕ, ЭКТОПИЯ СЕРДЦА, ОТСУТСТВИЕ НИЖНЕЙ ЧАСТИ ГРУДИНЫ С ДЕФЕКТАМИ ДИАФРАГМЫ И ПЕРИКАРДА)
DOI:
10.24110/0031-403X-2022-1
DOI:
10.24110/0031-403X-2022-101-1-214-217
Language:
Unknown
Publisher:
Pediatria, Ltd.
Publication Date:
2022
