| Literature DB >> 21416043 |
M Al-Haggar1, S Yahia, D Abdel-Hadi, F Grill, A Al Kaissi.
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.Entities:
Keywords: Gestational diabetes mellitus; Potter's syndrome; Sirenomelia; Symelia apus
Mesh:
Year: 2010 PMID: 21416043 PMCID: PMC3052805
Source DB: PubMed Journal: Afr Health Sci ISSN: 1680-6905 Impact factor: 0.927