Co-occurrence of Moyamoya syndrome and Kartagener syndrome caused by the mutation of DNAH5 and DNAH11: a case report

BACKGROUND: Kartagener syndrome is an autosomal recessive inherited disorder of primary ciliary dyskinesia. Moyamoya syndrome refers to a moyamoya angiopathy associated with other neurological and/or extra-neurological symptoms, or due to a well identified acquired or inherited cause. We herein repo...

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Detaylı Bibliyografya
Yayımlandı:BMC Neurol
Asıl Yazarlar: Zhang, Lili, Feng, Xungang, Zhang, Junhu, Hao, Yanlei, Wang, Yuzhong
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2020
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7448357/
https://ncbi.nlm.nih.gov/pubmed/32847546
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-020-01895-x
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