Hereditary Syndromes With Auditory and Dermatological Manifestations

William B. Reed

Archives of Dermatology · 1967 · 34 citations · 16 references

Concepts

TL;DR

Congenital sensorineural deafness frequently co‑occurs with hereditary keratinization and ectodermal disorders such as pili torti, onychodystrophy, keratosis palmaris et plantaris, and syndromes including Refsum, Cockayne, Hunter, Laurance‑Moon‑Bardet‑Biedl, xeroderma pigmentosa, and hidrotic ectodermal dysplasia, often presenting with hair, nail, and ear abnormalities. We identified four patients with pili torti and partial alopecia, showing autosomal dominant inheritance, and one Klein‑Waardenburg case with malformed ears and postauricular sinus tracts.

Abstract

Congenital deafness may be associated with hereditary disorders of keratinization. Pili torti, twisted hair, was first reported by Bjornstad with sensorineural deafness. We have found four similar patients with partial alopecia from pili torti. The inheritance appears to be autosomal dominant in character. Congenital deafness of the sensorineural type also has been noted with onychodystrophy, ainhum, and keratosis palmaris et plantaris. Hereditary disorders with important dermatological neurological complications may show an associated deafness. These include Refsum's, Cockayne's, Hunter's, and Laurance-Moon-Bardet-Biedl syndromes, xeroderma pigmentosa, and hidrotic ectodermal dysplasia. Congenital malformations sometimes from hereditary causes may show abnormal implantations of hair (Treacher-Collins syndrome), nail dystrophy (Turner's syndrome), and malformed ears with ear pits and sinus tracts. One patient with Klein-Waardenburg syndrome was noted to have malformed ears with postauricular sinus tracts.

References

16