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Items: 3

1.

Deafness dystonia syndrome

Males with deafness-dystonia-optic neuronopathy (DDON) syndrome have prelingual or postlingual sensorineural hearing impairment in early childhood, slowly progressive dystonia or ataxia in the teens, slowly progressive decreased visual acuity from optic atrophy beginning at approximately age 20 years, and dementia beginning at approximately age 40 years. Psychiatric symptoms such as personality change and paranoia may appear in childhood and progress. The hearing impairment appears to be consistent in age of onset and progression, whereas the neurologic, visual, and neuropsychiatric signs vary in degree of severity and rate of progression. Females may have mild hearing impairment and focal dystonia. [from GeneReviews]

MedGen UID:
162903
Concept ID:
C0796074
Disease or Syndrome
2.

Autosomal dominant nonsyndromic hearing loss 9

DFNA9 is an autosomal dominant adult-onset form of progressive sensorineural hearing loss associated with variable vestibular dysfunction (summary by Robertson et al., 2006). [from OMIM]

MedGen UID:
371327
Concept ID:
C1832425
Disease or Syndrome
3.

Postlingual sensorineural hearing impairment

A form of sensorineural hearing impairment with onset after the acquisition of speech. [from HPO]

MedGen UID:
870217
Concept ID:
C4024654
Pathologic Function
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