Author/Authors :
Al-Haggar, M Mansoura University Children s Hospital - Pediatrics Department, Genetic unit, Egypt , Yahia, S Mansoura University Children s Hospital - Pediatrics Department, Genetic unit, Egypt , Abdel-Hadi, D Mansoura University Children s Hospital - Pediatrics Department, Genetic unit, Egypt , Grill, F Orthopaedic Hospital of Speising - Paediatric orthopaedic surgery, Austria , Al Kaissi, A Orthopaedic Hospital of Speising - Paediatric orthopaedic surgery, Austria , Al Kaissi, A Ludwig Boltzmann Institute of Osteology - AUVA Trauma Centre Meidling, Hanusch Hospital of WGKK, Hanusch Hospital - 4th Medical Department, Austria
Abstract :
We report one case of a fetus of sirenomelia sequence with Potters syndrome which showed oligohydramnios and symelia apus. The infant showed absent urinary tract and external genitalia, the legs were fused by skin and had separate bones associated with Potter s syndrome. The mother had a history of gestational diabetes mellitus.
Keywords :
Sirenomelia , Potter s syndrome , Symelia apus , Gestational diabetes mellitus
