| Literature DB >> 1532426 |
M Sharland1, N R Bleach, P D Goberdhan, M A Patton.
Abstract
A family is presented with autosomal dominant progressive palmoplantar hyperkeratosis, which is invariably associated with a slowly progressive, bilateral, high frequency, sensorineural hearing loss. The family show no other ectodermal abnormality. The differential diagnosis and possible mechanisms are discussed. This family appears to represent a unique variant in the hyperkeratosis-deafness association.Entities:
Mesh：
Year: 1992 PMID： 1532426 PMCID： PMC1015822 DOI： 10.1136/jmg.29.1.50
Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318