Retinitis pigmentosa with sensorineural deafness.
- Specialty
- Ophthalmology
- Subspecialty
- Ophthalmology / Inherited retinal disease
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes, deafness from birth in type 1
- Gene(s) involved
- ADGRV1, ARSG, CDH23, CIB2, CLRN1, HARS, MYO7A, PCDH15, USH1C, USH1G, USH2A, WHRN
- Alternative names & eponyms
- Hallgren syndrome
Etiology & mechanism
Ciliary and stereocilia protein defects.
Gene(s) involved (12)
Symptoms & signs (6)
In plain terms, someone with Usher syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
1 shared
Alström syndrome
progressive vision loss
1 shared
Barakat syndrome
sensorineural deafness
1 shared
Brown–Vialetto–Van Laere syndrome
sensorineural deafness
1 shared
Congenital rubella syndrome
cataract
1 shared
EAST syndrome
sensorineural deafness
1 shared
Epstein syndrome
cataract
1 shared
Fuchs heterochromic iridocyclitis syndrome
cataract
1 shared
KID syndrome
sensorineural deafness
1 shared
Knobloch syndrome
cataract
1 shared
LEOPARD syndrome
sensorineural deafness
Shares genes with
None.
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