Clinical and molecular characterization of craniofrontonasal syndrome: new symptoms and novel pathogenic variants in the EFNB1 gene

BACKGROUND: Craniofrontonasal syndrome (CFNS) is a rare X-linked disorder that results from pathogenic variants in the EFNB1 gene. The syndrome paradoxically presents with greater severity of the symptoms in heterozygous females than hemizygous males. RESULTS: We have recruited and screened a female...

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Detalles Bibliográficos
Autores principales: Bukowska-Olech, Ewelina, Gawliński, Paweł, Jakubiuk-Tomaszuk, Anna, Jędrzejowska, Maria, Obersztyn, Ewa, Piechota, Michał, Bielska, Marta, Jamsheer, Aleksander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236199/
https://www.ncbi.nlm.nih.gov/pubmed/34174922
http://dx.doi.org/10.1186/s13023-021-01914-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236199/
https://www.ncbi.nlm.nih.gov/pubmed/34174922
http://dx.doi.org/10.1186/s13023-021-01914-1

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