A CASE OF A RARE CONGENITAL DEFECT OF THE MUSCULOSKELETAL SYSTEM – SIRENOMELIA IN COMBINATION WITH MEGACYSTIS AND A SINGLE UMBILICAL ARTERY

Main Article Content

Наталия Игоревна Андрюк
Ольга Аркадьевна Соловьева
Светлана Леонидовна Стопичева
Людмила Викторовна Абрамова
Светлана Ивановна Елгина
Елена Владимировна Рудаева
Кира Борисовна Мозес
Вадим Гельевич Мозес

Abstract

Sirenomelia (mermaid syndrome) is a congenital pathology that occurs due to a violation of the blood supply to the embryo. It is characterized by fusion of the lower extremities in combination with agenesis of the kidneys, aplasia of the sacrum, rectum and bladder. The frequency of occurrence is 1 per 60 thousand newborns, the sex ratio is male / female 2.7 : 1. Sirenomelia does not belong to an inherited anomaly, most cases are sporadic, so the risk of relapse is not significant. This publication is devoted to the early diagnosis of a congenital malformation of the musculoskeletal system - sirenomelia in combination with megacystis and a single umbilical artery.

Keywords

sirenomilia, the only artery of the umbilical cord, a congenital malformation of the fetus

Author Biographies

Наталия Игоревна Андрюк,

doctor of the ultrasound diagnostics department N 2

Ольга Аркадьевна Соловьева,

head of the department of ultrasound diagnostics N 2

Светлана Леонидовна Стопичева,

doctor, department of ultrasound diagnostics N 2

Людмила Викторовна Абрамова,

doctor of the ultrasound diagnostics department N 2

Светлана Ивановна Елгина,

doctor of medical sciences, docent, professor of the department of obstetrics and gynecology named after G.A. Ushakova

Елена Владимировна Рудаева,

candidate of medical sciences, docent, docent of the department of obstetrics and gynecology named after G.A. Ushakova

Кира Борисовна Мозес,

assistant of the department of outpatient therapy and nursing

Вадим Гельевич Мозес,

doctor of medical sciences, professor, deputy chief physician for scientific activities

Article Details

Information about financing and conflict of interests

The study had no sponsorship.
The authors declare that they have no apparent or potential conflicts of interest related to the publication of this article.

How to Cite

Андрюк, Н. И., Соловьева, О. А., Стопичева, С. Л., Абрамова, Л. В., Елгина, С. И., Рудаева, Е. В., Мозес, К. Б., & Мозес, В. Г. (2023). A CASE OF A RARE CONGENITAL DEFECT OF THE MUSCULOSKELETAL SYSTEM – SIRENOMELIA IN COMBINATION WITH MEGACYSTIS AND A SINGLE UMBILICAL ARTERY. Mother and Baby in Kuzbass, 24(4), 74-76. https://doi.org/10.24412/2686-7338-2023-4-74-76

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