Distinct severity of phenotype in Hajdu-Cheney syndrome: a case report and literature review

BACKGROUND: Hajdu-Cheney syndrome (HCS) is a rare inherited skeletal disorder caused by pathogenic mutations in exon 34 of NOTCH2. Its highly variable phenotypes make early diagnosis challenging. In this paper, we report a case of early-onset HCS with severe phenotypic manifestations but delayed dia...

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Detalles Bibliográficos
Autores principales: Zeng, Chunhua, Lin, Yunting, Lu, Zhikun, Chen, Zhen, Jiang, Xiaoling, Mao, Xiaojian, Liu, Zongcai, Lu, Xinshuo, Zhang, Kangdi, Yu, Qiaoli, Wang, Xiaoya, Huang, Yonglan, Liu, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060511/
https://www.ncbi.nlm.nih.gov/pubmed/32143606
http://dx.doi.org/10.1186/s12891-020-3181-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060511/
https://www.ncbi.nlm.nih.gov/pubmed/32143606
http://dx.doi.org/10.1186/s12891-020-3181-0

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