Autosomal dominant palmoplantar hyperkeratosis and sensorineural deafness in three generations.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 1532426.
- Also identified by PMC identifier 1015822.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
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.
Medical subject headings
- Deafness
- Keratoderma, Palmoplantar