Cargando…
The blended phenotype of a germline RIT1 and a mosaic PIK3CA variant
We report a patient with a germline RIT1 and a mosaic PIK3CA variant. The diagnosis of the RASopathy was confirmed by targeted sequencing following the identification of transient cardiomyopathy in a patient with PIK3CA-related overgrowth spectrum (PROS). Our observation confirms that the PIK3CA gai...
Autores principales: | Berland, Siren, Jareld, Jørgen, Hickson, Nicholas, Schlecht, Helene, Houge, Gunnar, Douzgou, Sofia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751416/ https://www.ncbi.nlm.nih.gov/pubmed/34887308 http://dx.doi.org/10.1101/mcs.a006121 |
Ejemplares similares
-
Cerebrofacial vascular metameric syndrome is caused by somatic pathogenic variants in PIK3CA
por: Sheppard, Sarah E., et al.
Publicado: (2021) -
Deep exploration of a CDKN1C mutation causing a mixture of Beckwith-Wiedemann and IMAGe syndromes revealed a novel transcript associated with developmental delay
por: Berland, Siren, et al.
Publicado: (2022) -
Pulmonary Vein Stenosis Associated with Germline PIK3CA Mutation
por: Yung, Delphine, et al.
Publicado: (2022) -
A Mosaic PIK3CA Mutation in a Moroccan Female: Exploring the Diagnostic Challenges of PIK3CA-Related Overgrowth Spectrum
por: Ahakoud, Mohamed, et al.
Publicado: (2023) -
Putting the Rit in cellular resistance: Rit, p38 MAPK and oxidative stress
por: Cai, Weikang, et al.
Publicado: (2013)