Conditions / Syndrome
Usher syndrome type 1G
info · Syndrome · ICD-10: H35.5
An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25.
Signs and symptoms
- Abnormal vestibular function
- Sensorineural hearing impairment
- Rod-cone dystrophy
- Hypoplasia of the nasal bone
Also known as: USH1G; Usher syndrome type IG