Sirenomelia in a preterm neonate: a rare and lethal congenital anomaly

Fatima Zahraa Belhaj, Mohamed Sellouti

PAMJ. 2025; 52:77. Published 17 Oct 2025 | doi:10.11604/pamj.2025.52.77.49478

A preterm neonate, born at 35 weeks of gestation with a birth weight of 2100 g and an Apgar score of 8/10, was delivered after an unmonitored pregnancy. Clinical examination revealed a single tapered appendage replacing the lower limbs, with absent musculature and soft tissue, highly suggestive of sirenomelia "mermaid syndrome". External genital organs were not identifiable. Complementary investigations demonstrated severe visceral malformations: renal ultrasound revealed bilateral renal agenesis, while echocardiography showed complex congenital heart anomalies. No craniofacial dysmorphism was noted. The infant initially presented with respiratory distress requiring CPAP support. At 12 hours of life, clinical deterioration occurred with temperature instability, feeding intolerance, and increasing oxygen requirements. Laboratory investigations showed a marked rise in C-reactive protein with progressive thrombocytopenia. Despite the initiation of broad-spectrum intravenous antibiotics, the clinical course rapidly worsened. The newborn developed refractory septic shock compounded by severe renal failure with hydro-electrolyte disturbances, leading to multiorgan dysfunction and death at 48 hours of life.
Corresponding author
Fatima Zahraa Belhaj, Children´s Hospital, Ibn Sina University Hospital Centre, Rabat, Morocco (belhajf199@gmail.com)


The Pan African Medical Journal (ISSN: 1937-8688) is a subsidiary of the Pan African Medical Journal. The contents of this journal is intended exclusively for professionals in the medical, paramedical and public health and other health sectors.

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