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A novel heterozygous variant of FOXJ1 in a Chinese female with primary ciliary dyskinesia and hydrocephalus: A case report and literature review
BACKGROUND: Primary ciliary dyskinesia (PCD) is a type of ciliary dyskinesia that is usually caused by autosomal recessive inheritance and can manifest as recurrent respiratory infections, bronchiectasis, infertility, laterality defects, and chronic otolaryngological disease. Although ependymal cili...
Autores principales: | Gao, Shiyang, Zhang, Qianwen, Feng, Biyun, Gu, Shili, Li, Zhiying, Sun, Lianping, Yao, Ru‐en, Yu, Tingting, Ding, Yu, Wang, Xiumin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496049/ https://www.ncbi.nlm.nih.gov/pubmed/37469238 http://dx.doi.org/10.1002/mgg3.2235 |
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