Prenatal diagnosis of single umbilical artery complicated by intrauterine growth retardation and preterm labor: Case report

Autor:	Mohamed E S Hamed, Ibrahim A. Abdelazim, Svetlana Shikanova, Mohannad AbuFaza, Gulmira Zhurabekova, Osama O Amer
Rok vydání:	2019
Předmět:	medicine.medical_specialty umbilical lcsh:Medicine Aneuploidy Case Report 030209 endocrinology & metabolism Prenatal diagnosis Umbilical cord 03 medical and health sciences 0302 clinical medicine Medicine 030212 general & internal medicine single Fetus business.industry Obstetrics Single umbilical artery lcsh:R intrauterine growth retardation medicine.disease Artery medicine.anatomical_structure embryonic structures Gestation Small for gestational age preterm business
Zdroj:	Journal of Family Medicine and Primary Care Journal of Family Medicine and Primary Care, Vol 8, Iss 6, Pp 2151-2154 (2019)
ISSN:	2249-4863
DOI:	10.4103/jfmpc.jfmpc_394_19
Popis:	Fetuses with single umbilical artery (SUA) at great risk of intrauterine growth retardation (IUGR), intrauterine fetal death (IUFD) and prematurity. A 24-years-old woman, 28 weeks' gestation, presented to the Ahmadi hospital, Kuwait, with history of preterm premature rupture of fetal membranes (PPROM). After exclusion of the PPROM, the ultrasound scan of the studied woman showed; asymmetrical IUGR with SUA. The diagnosis of SUA confirmed by the color flow Doppler. She delivered spontaneously at 36 weeks+2, and a cut section in the umbilical cord done to confirm the diagnosis of SUA. The congenital and chromosomal abnormalities of the studied neonate excluded after normal pelvi-abdominal, brain ultrasound and normal karyotyping (46, xx); respectively. The prenatal diagnosed SUA in the studied cases associated with IUGR, preterm labor (PTL) and small for gestational age (SGA). SUA can be considered a marker of diagnosable congenital fetal malformation (CFM) and aneuploidy.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8311ae2271946844cc2bee332c56d7f2 https://doi.org/10.4103/jfmpc.jfmpc_394_19 Zobrazit plný text záznamu Plný text ve formátu PDF Plný text ve formátu HTML
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