Mermaid Syndrome: Virtually No Hope for Survival
Overview
Pediatrics
Affiliations
Sirenomelia, also called the mermaid syndrome is a severe malformation involving multiple organs and characterized by partially or completely developed lower extremities fused by the skin. The birth of a "mermaid" is very rare (1.2-4.2 cases for 100,000 births); most are stillborn, or die at or shortly after birth. The case of a living female neonate with dipodic simelia (fusion of well-developed legs) is presented. No prenatal diagnosis was made and the newborn had an uneventful neonatal course following Cesarean section delivery. The complex and striking malformation was obvious at birth and further evaluation revealed very poorly functioning kidneys, associated with abnormal anorectum, urogenital tract, and external genitalia, as well as a pelvic malformation. Supportive care was applied because of the poor prognosis and the child died at 7 weeks of age, due to renal failure.
Sirenomelia or mermaid syndrome with a cleft lip in a Tanzanian newborn: a case report.
Wilfred Z, Magitta N J Med Case Rep. 2024; 18(1):224.
PMID: 38706003 PMC: 11071204. DOI: 10.1186/s13256-024-04549-5.
Surgical Management of Sirenomelia: A Case Study.
Bhagat N, Patel A, Gross J, Borschel G Plast Reconstr Surg Glob Open. 2023; 11(9):e5275.
PMID: 38155744 PMC: 10754566. DOI: 10.1097/GOX.0000000000005275.
Sirenomelia: two case reports.
Shojaee A, Ronnasian F, Behnam M, Salehi M J Med Case Rep. 2021; 15(1):217.
PMID: 33902682 PMC: 8077960. DOI: 10.1186/s13256-021-02699-4.