Genetic and Metabolic Deafness |
Contents
Chapter | 1 |
Chapter | 7 |
Dominant Unilateral Sensorineural Deafness | 13 |
Copyright | |
39 other sections not shown
Common terms and phrases
abnormalities affected persons affected sibs Alport syndrome anomalies Arch ataxia Audiograms Auditory System autosomal dominant autosomal recessive autosomal recessive inheritance bilateral Birth Defects cent childhood cleft CLINICAL FINDINGS Physical clude cochlear conduction deafness conductive hearing loss congenital deafness congenital sensorineural deafness described DIAGNOSIS disease disorder distal dominant transmission drome dysostosis dysplasia exhibited facial FINDINGS Physical Findings Fraser frequencies Genet Gorlin hearing aid HEREDITY hypertelorism hypoplasia Integumentary System kindred Konigsmark LABORATORY FINDINGS Roentgenograms Laryngol male malformed mental retardation mild mixed hearing loss moderate muscle myopia nasal nerve Nervous System neural deafness normal noted Ocular System onset Ophthalmol optic atrophy Otol otosclerosis PATHOLOGY patients Pediatr Pedigree phalanges preauricular pits PROGNOSIS progressive sensorineural Radiograph renal reported retinitis pigmentosa sensori sensorineural deafness sensorineural hearing loss severe sensorineural showed skeletal sorineural stapes Stockh studies SUMMARY Characteristics temporal bone tients tion TREATMENT Vestibular System vestibular tests Waardenburg's syndrome X-linked