Ultrasonographic findings and prenatal diagnosis of Jacobsen syndrome: A case report and review of the literature

RATIONALE: Jacobsen syndrome (JBS) is a rare chromosomal disorder with variable phenotypic expressivity, which is usually diagnosed in infancy and childhood based on clinical examination and hematological and cytogenetic findings. Prenatal diagnosis and fetal ultrasonographic findings of JBS are rar...

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Detalles Bibliográficos
Autores principales: Chen, Shuang, Wang, Ruixue, Zhang, Xinyue, Li, Leilei, Jiang, Yuting, Liu, Ruizhi, Zhang, Hongguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
5600
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946260/
https://www.ncbi.nlm.nih.gov/pubmed/31895838
http://dx.doi.org/10.1097/MD.0000000000018695

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946260/
https://www.ncbi.nlm.nih.gov/pubmed/31895838
http://dx.doi.org/10.1097/MD.0000000000018695

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