Congenital Hereditary Facial Paralysis-Variable Hearing Loss Syndrome

Congenital Hereditary Facial Paralysis-Variable Hearing Loss Syndrome(来自ICD-11)

别称:

Congenital Hereditary Facial Paralysis-Variable Deafness Syndrome

Congenital Hereditary Facial Palsy with Variable Hearing Loss

Congenital Hereditary Facial Paralysis with Variable Deafness

Congenital Hereditary Facial Palsy with Variable Deafness

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Congenital Hereditary Facial Paralysis-Variable Hearing Loss Syndrome, is also known as congenital hereditary facial paralysis-variable deafness syndrome. An important gene associated with Congenital Hereditary Facial Paralysis-Variable Hearing Loss Syndrome is HOXB1 (Homeobox B1).

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