Perrault Syndrome 2 (PRLTS2)

Alias:
Prlts2
Xx Gonadal Dysgenesis-Deafness Syndrome-Progressive Neurological Manifestations
Perrault Syndrome, Type 2
Perrault Syndrome Type 2
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Perrault Syndrome 2, also known as prlts2, is related to sensorineural hearing loss and perrault syndrome. An important gene associated with Perrault Syndrome 2 is HARS2 (Histidyl-TRNA Synthetase 2, Mitochondrial), and among its related pathways/superpathways are Primary ovarian insufficiency and tRNA Aminoacylation. Affiliated tissues include ovary, and related phenotypes are sensorineural hearing impairment and streak ovary
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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8
38
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Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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