Understanding Hereditary Nerve Deafness
- 1 January 1967
- journal article
- research article
- Published by American Medical Association (AMA) in JAMA Otolaryngology–Head & Neck Surgery
- Vol. 85 (1) , 23-40
- https://doi.org/10.1001/archotol.1967.00760040025007
Abstract
THE PROBLEM of hereditary nerve deafness is indeed a complex and challenging one. With the otologist having very little to offer medically or surgically, except in the rare case of a conductive malformation combined with the sensorineural loss, treatment today is limited largely to diagnosis and rehabilitation. Because some forms of hereditary deafness may develop insidiously and not become clinically apparent until later in life, because hereditary nerve deafness is sometimes associated with other abnormalities which may overshadow it, and because hereditary factors may be concealed, it is difficult to accurately estimate the frequency of this disease. It appears that hereditary deafness is actually a fairly common disease entity, possibly occurring somewhere between 1 in 2,000 and 1 in 6,000 births. Of all cases of congenital deafness, including deafness secondary to rubella, birth injury, and erythroblastosis, about one third to one half seem to be due to hereditary factors. AtThis publication has 18 references indexed in Scilit:
- Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden deathPublished by Elsevier ,2004
- URTICARIA, DEAFNESS, AND AMYLOIDOSIS: A NEW HEREDO-FAMILIAL SYNDROMEQJM: An International Journal of Medicine, 1962
- A New Hereditary Syndrome – Sex-linked Deaf-mutism Associated with Total AlbinismHuman Heredity, 1962
- Hereditary nephropathy, deafness and renal foam cellsThe American Journal of Medicine, 1961
- Familial pulmonary stenosis and deaf-mutism: Clinical and genetic considerationsAmerican Heart Journal, 1958
- SYNDROME OF HEREDITARY HEMATURIA, NEPHROPATHY AND DEAFNESS1958
- A NEW SYNDROME COMBINING DEVELOPMENTAL ANOMALIES OF THE EYELIDS, EYEBROWS AND NOSE ROOT WITH PIGMENTARY DEFECTS OF THE IRIS AND HEAD HAIR AND WITH CONGENITAL DEAFNESS - DYSTOPIA-CANTHI MEDIALIS ET PUNCTORUM LACRIMALIUM LATEROVERSA, HYPERPLASIA SUPERCILII MEDIALIS ET RADICIS NASI, HETEROCHROMIA IRIDUM TOTALIS SIVE PARTIALIS, ALBINISMUS CIRCUMSCRIPTUS (LEUCISMUS, POLIOSIS), ET SURDITAS CONGENITA (SURDIMUTITAS)1951
- Deafness and the Laurence-Moon-Biedl SyndromeBritish Journal of Ophthalmology, 1950
- FAMILIAL MYOCLONUS EPILEPSY ASSOCIATED WITH DEAF-MUTISM IN A FAMILY SHOWING OTHER PSYCHOBIOLOGICAL ABNORMALITIESAnnals of Eugenics, 1937
- Experimental researches on the origin of the acoustic ganglion in amphibian embryosJournal of Experimental Zoology, 1935