Cargando…
An Unusual Presentation of Cardiofaciocutaneous Syndrome Diagnosed Through Whole Genome Sequencing: A Case Report
Cardiofaciocutaneous syndrome is a rare, sporadic disease caused by germline mutations in the Ras/MAPK (mitogen-activated protein kinase) pathway. Patients usually present with craniofacial anomalies, cardiac defects, and neurocutaneous abnormalities. The features of cardiofaciocutaneous syndrome ov...
Autores principales: | Alhalak, Rouzy, Al-Haideri, Mohammed H, Khan, Arif |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10022705/ https://www.ncbi.nlm.nih.gov/pubmed/36938251 http://dx.doi.org/10.7759/cureus.35021 |
Ejemplares similares
-
Cardiofaciocutaneous Syndrome: A Rare Entity
por: Pavithra, S, et al.
Publicado: (2012) -
Bladder leiomyoma treated with transurethral resection of bladder tumor (TURBT): Case report
por: AlHalak, Rouzy, et al.
Publicado: (2022) -
Infantile epileptic spasms syndrome in children with cardiofaciocutanous syndrome: Clinical presentation and associations with genotype
por: Kenney‐Jung, Daniel L., et al.
Publicado: (2022) -
Diet-Responsive Hypercholesterolemia With Cardiofaciocutaneous Syndrome Type 3
por: Patni, Nivedita, et al.
Publicado: (2021) -
Identifying the genetic causes of phenotypically diagnosed Pakistani mucopolysaccharidoses patients by whole genome sequencing
por: Gul, Rutaba, et al.
Publicado: (2023)