Cargando…
Molecular screening strategies for NF1-like syndromes with café-au-lait macules
Multiple café-au-lait macules (CALM) are usually associated with neurofibromatosis type 1 (NF1), one of the most common hereditary disorders. However, a group of genetic disorders presenting with CALM have mutations that are involved in human skin pigmentation regulation signaling pathways, includin...
Autores principales: | Zhang, Jia, Li, Ming, Yao, Zhirong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112360/ https://www.ncbi.nlm.nih.gov/pubmed/27666661 http://dx.doi.org/10.3892/mmr.2016.5760 |
Ejemplares similares
-
Bardet–Biedl Syndrome with Café-au-Lait Macule: Association or Coincidence?
por: Tomar, Suyash S., et al.
Publicado: (2020) -
Plexiform Neurofibroma Overlying Giant Café-au-lait Macule
por: Choudhary, Sanjiv V., et al.
Publicado: (2017) -
An approach to café au lait macules in primary care setting
por: Almuhaidib, Seereen R., et al.
Publicado: (2021) -
Laser treatment for Cafe-au-lait Macules: a systematic review and meta-analysis
por: Guo, Zi-Zhen, et al.
Publicado: (2023) -
Type VIII - Ehlers Danlos Syndrome with café-au-lait macules: A Rare Variant
por: Bhat, Ramesh M, et al.
Publicado: (2014)