Neonatal hereditary spherocytosis caused by a de novo frameshift mutation of the SPTB gene characterized by hydrops fetalis: A case report

RATIONALE: The etiology of non-immune hydrops fetalis is complex, and its prognosis is poor. One of its main causes is anemia. There are few reports on hydrops fetalis due to anemia caused by hereditary spherocytosis (HS), especially regarding its occurrence in the neonatal period. Thus, we report o...

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Detalles Bibliográficos
Autores principales: Zhang, Yimin, Shao, Shuming, Liu, Jie, Zeng, Chaomei, Han, Ye, Zhang, Xiaorui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
6200
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282131/
https://www.ncbi.nlm.nih.gov/pubmed/33761640
http://dx.doi.org/10.1097/MD.0000000000024804

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282131/
https://www.ncbi.nlm.nih.gov/pubmed/33761640
http://dx.doi.org/10.1097/MD.0000000000024804

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