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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2021
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| Materias: | |
| 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 |