TWNK Gene Associated Perrault Syndrome Patient with Neurological Features
Journal of the Korean Neurological Association
;
: 137-140, 2023.
Article
Dans Coréen
| WPRIM
| ID: wpr-977060
ABSTRACT
Perrault syndrome 5 is a rare autosomal recessive disorder that is characterized by the association of sensorineural hearing loss and ovarian dysgenesis in females with diversity of neurologic deficits due to variants of twinkle mtDNA helicase (TWNK) gene. Since neurologic deficits develop gradually, patient is often misdiagnosed with other neurological disease during early age. Herein, we report a case of genetically diagnosed Perrault syndrome 5.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
langue:
Coréen
Texte intégral:
Journal of the Korean Neurological Association
Année:
2023
Type:
Article
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