Expanding the PURA syndrome phenotype with manifestations in a Japanese female patient.
Hum Genome Var
; 9(1): 11, 2022 Apr 19.
Article
em En
| MEDLINE
| ID: mdl-35440576
ABSTRACT
We report on a 15-year-old Japanese female patient with hypotonia and global developmental delay from the neonatal period who was revealed to carry a known pathogenic PURA variant (NM_005859.5c.697_699del, p.Phe233del) by whole-exome sequencing. She had previously unreported clinical features, including a rectovestibular fistula, extremely short stature, and underweight, expanding the known phenotype of PURA syndrome.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Idioma:
En
Revista:
Hum Genome Var
Ano de publicação:
2022
Tipo de documento:
Article