Prenatal diagnosis of a rare variant of harlequin ichthyosis with literature review

BACKGROUND: Harlequin ichthyosis (HI) is a rare and severe genetic skin disorder that occurs within the developing foetus. Due to the extremely poor prognosis, prenatal diagnosis becomes very important, especially for foetuses with no family history. There are few reports on prenatal diagnosis in Pu...

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Detalles Bibliográficos
Autores principales: Zhou, Yi, Li, Liang, Wang, Ling, Zhang, Chaoxue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7981911/
https://www.ncbi.nlm.nih.gov/pubmed/33743627
http://dx.doi.org/10.1186/s12880-021-00586-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7981911/
https://www.ncbi.nlm.nih.gov/pubmed/33743627
http://dx.doi.org/10.1186/s12880-021-00586-4

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