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Klippel–Trenaunay and Sturge–Weber Overlap Syndrome with KRAS and GNAQ mutations

Patients with combined phenotypes of Sturge–Weber syndrome and Klippel–Trenaunay syndrome have been reported, though the underlying genetic spectrum in these individuals remains to be elucidated. We reported the patient presenting with Klippel–Trenaunay and Sturge–Weber overlap syndrome in mainland...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Ann Clin Transl Neurol
Egile Nagusiak: He, Ruojie, Liao, Songjie, Yao, Xiaoli, Huang, Ruxun, Zeng, Jinsheng, Zhang, Jian, Yu, Jian
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: John Wiley and Sons Inc. 2020
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC7359123/
https://ncbi.nlm.nih.gov/pubmed/32613723
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51106
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