Advertisement!
Author Information Pack
Editorial Board
Submit article
Special Issue
Editor's selection process
Join as Reviewer/Editor
List of Reviewer
Indexing Information
Most popular articles
Purchase Single Articles
Archive
Free Online Access
Current Issue
Recommend this journal to your library
Advertiser
Accepted Articles
Search Articles
Email Alerts
FAQ
Contact Us
Indian Journal of Forensic Medicine and Pathology

Volume  7, Issue 2, April - June 2014, Pages 85-88
 

Case Report

Sirenomelia: Mermaid Syndrome – A Rare Autopsy Case Report

Anuradha G. Patil, Anita M., Shabnam Karangadan, Sainath K. Andola

*Professor, **Associate Professor, ***Resident, ****Professor and Head of Department, Department of Pathology, M.R. Medical College, Gulbarga, Karnataka, India.

Choose an option to locate / access this Article:
90 days Access
Check if you have access through your login credentials.        PDF      |
|

Open Access: View PDF

DOI:

Abstract

Sirenomelia, the Mermaid Syndrome is a rare and lethal congenital anomaly with an incidence of one in 60,000 pregnancies. Sirenomelia is characterized by fusion of the lower limbs, commonly associated with renal agenesis, absent external genitalia and other gastrointestinal defects. We report a case of sirenomelia in a stillborn 26 wks fetus received for autopsy. Apart from the characteristic features it was also associated with single umbilical artery, potter’s facies and hypoplasia of various internal organs. Ultrasound may be useful in the early antenatal detection of this anomaly however coexisting oligohydramnios as in this case makes the visualisation of caudal extremity difficult. Early prenatal diagnosis should be the aim to minimize the trauma related to the termination of pregnancy at advanced gestation.

Keywords: Sirenomelia; Mermaid syndrome.


Corresponding Author : Anuradha G. Patil