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Antenatal diagnosis of Seckel Syndrome: a rare case report

INTRODUCTION: Seckel Syndrome is a rare autosomal recessive disorder characterized by dwarfism, microcephaly and the absence of visceral malformations. CASE REPORT: we observed sonographic features of a Seckel Syndrome, in a patient during the 24th week of pregnancy. Her family history was negative...

詳細記述

保存先:
書誌詳細
出版年:J Prenat Med
主要な著者: Vascone, Carmine, Di Meglio, Filippo, Di Meglio, Letizia, Turco, Luigi Carlo Lo, Vitale, Salvatore Giovanni, Cignini, Pietro, Marilli, Ilaria, Rapisarda, Agnese Maria Chiara, Valenti, Gaetano, Cianci, Stefano
フォーマット: Artigo
言語:Inglês
出版事項: CIC Edizioni Internazionali 2014
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4510566/
https://ncbi.nlm.nih.gov/pubmed/26266004
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