Pendred syndrome
Pendred syndrome: autosomal recessive genetic disorder (chromosome 7q31), characterized by congenital sensorineural deafness and goitre.
Pendred syndrome: autosomal recessive genetic disorder (chromosome 7q31), characterized by congenital sensorineural deafness and goitre.
Vaughan Pendred (1869–1946) was an English GP. Pendred first described the syndrome of bilateral sensorineural hearing loss with goitre (Pendred syndrome)