Prenatal diagnosis of 18p deletion and 8p trisomy syndrome: literature review and report of a novel case

• Автори: Maria Papamichail (Автор), Anna Eleftheriades (Автор), Emmanouil Manolakos (Автор), Adamantia Papamichail (Автор), Panagiotis Christopoulos (Автор), Gwendolin Manegold-Brauer (Автор), Makarios Eleftheriades (Автор)
• Формат: Книга
• Опубліковано: BMC, 2024-04-01T00:00:00Z.
• Предмети: article
• Онлайн доступ: Connect to this object online.

Abstract 18p deletion syndrome constitutes one of the most frequent autosomal terminal deletion syndromes, affecting one in 50,000 live births. The syndrome has un-specific clinical features which vary significantly between patients and may overlap with other genetic conditions. Its prenatal descrip...