Cochleosaccular degeneration with progressive cataracts

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Cochleosaccular degeneration with progressive cataracts
Autosomal dominant - en.svg
Specialty Medical genetics, Audiology
Usual onsetAdulthood
Frequencyrare
Deaths1, which may or may not have been related to the disorder itself.

Cochleosaccular degeneration with progressive cataracts, also known as autosomal dominant progressive sensorineural hearing loss and cataracts [1] is a rare genetic disorder characterized by the adult-onset combination of cochleosaccular degeneration and progressive cataract [2] which is transmitted as an autosomal dominant trait for generations in entire families, [3] essentially resulting in familial deafblindness. [4] Additional features include unstable gait. [5] Only 15 cases from 2 multi-generational families in the United States and Italy (respectively) have been described in medical literature. [5]

Cases

References

  1. "Autosomal Dominant Progressive Sensorineural Deafness and Cataract Syndrome". DoveMed. Retrieved 14 September 2022.
  2. "Orphanet: Cochleosaccular degeneration cataract syndrome". www.orpha.net. Retrieved 14 September 2022.
  3. "Deafness progressive cataract autosomal dominant". Global Genes. Retrieved 14 September 2022.
  4. "Cochleosaccular degeneration of the inner ear and progressive cataracts – About the Disease – Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Archived from the original on 3 February 2017. Retrieved 14 September 2022.
  5. 1 2 "Clinical Synopsis – 120040 – Cochleosaccular Degeneration with Progressive Cataracts – OMIM". omim.org. Retrieved 14 September 2022.
  6. Nadol, J. B.; Burgess, B. (September 1982). "Cochleosaccular degeneration of the inner ear and progressive cataracts inherited as an autosomal dominant trait". The Laryngoscope. 92 (9 Pt 1): 1028–1037. doi: 10.1288/00005537-198209000-00013 . ISSN   0023-852X. PMID   7121157. S2CID   38674246.
  7. Guala, A.; Germinetti, V.; Sebastiani, F.; Silengo, M. C. (June 1992). "A syndrome of progressive sensorineural deafness and cataract inherited as an autosomal dominant trait". Clinical Genetics. 41 (6): 293–295. doi:10.1111/j.1399-0004.1992.tb03400.x. ISSN   0009-9163. PMID   1623624. S2CID   30225499.