J Med Genet. 1992 Jan;29(1):50-2.

Autosomal dominant palmoplantar hyperkeratosis and sensorineural deafness in three generations.

Sharland M, Bleach NR, Goberdhan PD, Patton MA.

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Department of Genetics, St George's Hospital Medical School, London.

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.

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J Med Genet. 1992 Jun;29(6):440.

PMID:: 1532426; [PubMed - indexed for MEDLINE]
PMCID:: PMC1015822

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Cited by 1 PubMed Central article

Palmoplantar hyperkeratosis and deafness. [J Med Genet. 1992]
Palmoplantar hyperkeratosis and deafness.
Verbov J. J Med Genet. 1992 Jun; 29(6):440.

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