Discordant phenotype caused by CASK mutation in siblings with NF1.
Hum Genome Var
; 6: 20, 2019.
Article
em En
| MEDLINE
| ID: mdl-31044082
With the advent of next-generation sequencing (NGS), a blended phenotype has been shown to be caused by multilocus molecular diagnosis. Here, we present siblings of neurofibromatosis type 1 (NF1) with discordant phenotypes. Further genetic investigation revealed that the younger sister had trisomy 8 mosaicism with a low ratio and a known pathogenic mutation in the CASK gene. This is the first report of a blended phenotype caused by NF1, CASK disorder, and trisomy 8 mosaicism.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Idioma:
En
Revista:
Hum Genome Var
Ano de publicação:
2019
Tipo de documento:
Article
País de afiliação:
Japão
País de publicação:
Reino Unido