K. Eisnecker
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View article: VP46.01: Arteriovenous malformation following uterine scar pregnancy
VP46.01: Arteriovenous malformation following uterine scar pregnancy Open
A 32-year-old patient (G2, P1) presented with vaginal bleeding two weeks after her last menstrual bleeding. Hemoglobin (Hb) was normal and beta-HCG level was negative. She had been treated by curettage for missed abortion three months befo…
View article: VP25.06: Anophthalmia due to a novel mutation in the SOX2 gene
VP25.06: Anophthalmia due to a novel mutation in the SOX2 gene Open
Anophthalmia is a rare congenital malformation with an estimated incidence of 0.04–0.18 in 10,000 births. It may occur as an isolated finding or part of syndromes. We herein describe a case of prenatally diagnosed anophthalmia due to a nov…
View article: VP26.11: Prenatal diagnosis of Aicardi syndrome: a case report
VP26.11: Prenatal diagnosis of Aicardi syndrome: a case report Open
Aicardi syndrome is a rare sporadic congenital disorder with x-linked dominant inheritance presenting with agenesis of the corpus callosum, central chorioretinal lacunae and infantile spasms. Additionally, all individuals present with brai…