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Abstract

Citation: Ann Clin Case Rep. 2017;2(1):1300.DOI: 10.25107/2474-1655.1300

Sirenomelia: A Rare Malformation

Ritika Khurana, Abhishek Arya and Prerna Batra

Department of Pediatrics, University College of Medical Sciences and Guru Tegh Bahadur Hospital, India

*Correspondance to: Prerna Batra 

 PDF  Full Text Case Report | Open Access

Abstract:

Sirenomelia, also known as ‘mermaid syndrome’, is a very rare congenital syndrome with an overall incidence of 1 in 1 lakh live births. It is a polymalformation disorder in which both the lower extremities of the baby are fused. There is no urinary bladder, no rectum, no vagina, no uterus; a colon of few inches is present. It is fatal by second or third day of life in most cases.

Keywords:

Mermaid baby; Sirenomelia; Caudal regression syndrome

Cite the Article:

Khurana R, Arya A, Batra P. Sirenomelia: A Rare Malformation. Ann Clin Case Rep. 2017; 2: 1300.

Journal Basic Info

  • Impact Factor: 5.253*
  • H-Index: 6
  • ISSN: 2474-1655
  • DOI: 10.25107/2474-1655
  • PubMed NLM ID: 101702800

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