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Autosomal recessive inheritance of Charcot‐Marie‐Tooth disease associated with sensorineural deafness
Author(s) -
Cornell J.,
Sellars S.,
Beighton P.
Publication year - 1984
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1984.tb00479.x
Subject(s) - tooth disease , autosomal recessive trait , sensorineural deafness , autosomal recessive inheritance , genetics , sensorineural hearing loss , medicine , consanguinity , inheritance (genetic algorithm) , x linked recessive inheritance , biology , hearing loss , x chromosome , audiology , gene
Three siblings with a combination of sensorineural deafness and the Charcot‐Marie‐Tooth syndrome have been investigated in a consanguineous Indian kindred. This syndrome, which to the best of our knowledge has not previously been reported, is probably inherited as an autosomal recessive trait.