Congenital hyperinsulinism and Poland syndrome in association with 10p13–14 duplication

[摘要] SummaryPoland syndrome (PS) is a rare congenital condition, affecting 1 in 30 000 live births worldwide, characterised by a unilateral absence of the sternal head of the pectoralis major and ipsilateral symbrachydactyly occasionally associated with abnorm

[学科分类] 内分泌与代谢学