In:
Pediatria. Journal named after G.N. Speransky, Pediatria, Ltd., Vol. 100, No. 1 ( 2021-02-15), p. 229-233
Abstract:
The article presents a case of a very rare malformations combination in a child born from multiple pregnancy (twins) after in vitro fertilization. The premature boy was born the second at 35,4 weeks by caesarean section for premature membranes rupture. The child had malformations of the thoracic vertebrae, ribs, kidneys and urinary system, esophageal atresia with tracheoesophageal fistula, characteristic for VACTERL association. At the same time, other anomalies of the sacral spine, lower extremities and lower urinary tract matched the classic caudal regression syndrome. The data obtained in recent years indicate that abnormalities in the same genes can cause VACTERL association and caudal regression syndrome. The standard approach in the treatment of such patients involves surgical correction of abnormalities to provide adequate vital functions of gas exchange, hemodynamics and digestion. The clinical observation published in this study demonstrates the success of this approach in a patient with a combination of VACTERL association and caudal regression syndrome.
Type of Medium:
Online Resource
ISSN:
0031-403X
,
1990-2182
Uniform Title:
КАУДАЛЬНАЯ РЕГРЕССИЯ И VACTERL-АССОЦИАЦИЯ У РЕБЕНКА ОТ МНОГОПЛОДНОЙ БЕРЕМЕННОСТИ (ДВОЙНЯ), НАСТУПИВШЕЙ ПОСЛЕ ПРИМЕНЕНИЯ ВСПОМОГАТЕЛЬНЫХ РЕПРОДУКТИВНЫХ ТЕХНОЛОГИЙ
DOI:
10.24110/0031-403X-2021-1
DOI:
10.24110/0031-403X-2021-100-1-229-233
Language:
Unknown
Publisher:
Pediatria, Ltd.
Publication Date:
2021
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