Georges Rameh
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VP32.01: Raine syndrome: case report and literature review of different antenatal imaging modalities Open
Raine syndrome (lethal osteosclerotic bone dysplasia) is a rare autosomal recessive disorder due to a mutation in FAM20C gene on chromosome 7p22.3 (around 50 cases are reported in the literature; 10 with antenatal findings described). We r…
Endometriosis and Epigenetics: What do we Know? Open
ObjectiveEndometriosis is a common gynecological condition with a pathogenesis that is multifactorial and not well understood.The aim of this review was to explore the multiplicity of epigenetic changes in the field of this disease. Main F…