Literature DB >> 9450850

Apparently new syndrome of sensorineural hearing loss, retinal pigment epithelium lesions, and discolored teeth.

J W Innis1, P A Sieving, P McMillan, R A Weatherly.   

Abstract

We report on a family with early-onset sensorineural hearing loss, abnormal retinal pigment epithelium granularity, accumulation of creamy-white lesions at the level of the retinal pigment epithelium particularly superior to the arcade, and selective discoloration (brown) of molars or canine deciduous teeth that follows an apparent autosomal recessive inheritance pattern. This appears to be a new syndrome that can be distinguished from the known otodental, oculo-acoustic and flecked retina syndromes by the occurrence of distinct dental and ocular abnormalities.

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Year:  1998        PMID: 9450850     DOI: 10.1002/(sici)1096-8628(19980106)75:1<13::aid-ajmg4>3.0.co;2-r

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  1 in total

1.  Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q.

Authors:  S Pieke-Dahl; C G Möller; P M Kelley; L M Astuto; C W Cremers; M B Gorin; W J Kimberling
Journal:  J Med Genet       Date:  2000-04       Impact factor: 6.318

  1 in total

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