SIRENOMELIA ASSOCIATED WITH HYPOPLASTIC LEFT HEART IN A NEWBORN

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dc.authoridturgut, hatice/0000-0002-0490-7852
dc.authoridKARAKURT, CEMŞIT/0000-0002-9246-8107;
dc.authorwosidturgut, hatice/IZQ-4154-2023
dc.authorwosidKARAKURT, CEMŞIT/ABE-2330-2020
dc.authorwosidGökçe, İsmail Kürşad/ABI-8128-2020
dc.contributor.authorTurgut, H.
dc.contributor.authorOzdemir, R.
dc.contributor.authorGokce, I. K.
dc.contributor.authorKarakurt, C.
dc.contributor.authorKaradag, A.
dc.date.accessioned2024-08-04T20:44:00Z
dc.date.available2024-08-04T20:44:00Z
dc.date.issued2017
dc.departmentİnönü Üniversitesien_US
dc.description.abstractSirenomelia, also known as mermaid malformation/ syndrome, is a rare, serious congenital anomaly characterized by variable degrees of fusion of the lower limbs and associated with severe malformations of vertebral, genitourinary, cardiovascular system and single umbilical artery. The first pregnancy of a 25-year-old woman resulted in one twin born by Cesarian section at 32 weeks' gestation, who was referred to our hospital with cyanosis, a congenital anomaly and respiratory distress. On physical examination, there was no urogenital region and anal fissure and gender was indeterminate. The arms were in adduction and wrist in flexion position with four fingers on the right hand and two fingers on the left hand. There was a single lower extremity with a webbed single foot and two toes consistent with sirenomelia type IV radiologically. Abdominal ultrasonography showed urogenital system agenesis and echocardiography detected hypoplastic left heart. However, the patient died 4 hours after birth. The other twin was followed for 1 week for nutrition and respiratory support and was then discharged without any problems.en_US
dc.identifier.doi10.1515/bjmg-2017-0001
dc.identifier.endpage94en_US
dc.identifier.issn1311-0160
dc.identifier.issue1en_US
dc.identifier.pmid28924546en_US
dc.identifier.scopus2-s2.0-85029649853en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage91en_US
dc.identifier.urihttps://doi.org/10.1515/bjmg-2017-0001
dc.identifier.urihttps://hdl.handle.net/11616/97974
dc.identifier.volume20en_US
dc.identifier.wosWOS:000410373900012en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherMacedonian Acad Sciences Artsen_US
dc.relation.ispartofBalkan Journal of Medical Geneticsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCaudal regression syndrome (CRS)en_US
dc.subjectHypoplastic left hearten_US
dc.subjectSirenomeliaen_US
dc.titleSIRENOMELIA ASSOCIATED WITH HYPOPLASTIC LEFT HEART IN A NEWBORNen_US
dc.typeArticleen_US

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