Cargando…
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...
Autores principales: | Zhang, Lili, Feng, Xungang, Zhang, Junhu, Hao, Yanlei, Wang, Yuzhong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448357/ https://www.ncbi.nlm.nih.gov/pubmed/32847546 http://dx.doi.org/10.1186/s12883-020-01895-x |
Ejemplares similares
-
Novel homozygous mutations of DNAH5 in Kartagener syndrome
por: Cheng, Xian-Dong, et al.
Publicado: (2021) -
Novel compound heterozygous mutations of DNAH5 identified in a pediatric patient with Kartagener syndrome: case report and literature review
por: Wang, Lina, et al.
Publicado: (2021) -
DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome
por: Liu, Sida, et al.
Publicado: (2019) -
DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease
por: Xia, Hong, et al.
Publicado: (2021) -
A Japanese Case of Primary Ciliary Dyskinesia with DNAH5 Mutations
por: Orimo, Mami, et al.
Publicado: (2019)