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5 entries match ENT & Hearing [C09] · Genetics & Heredity [K01.900.300]
1951 CE
#4154.4
A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair with congenital deafness.
“Waardenburg’s syndrome”.
1896 CE
#3840.1
Deaf-mutism and goitre.
Pendred syndrome, a genetic disorder leading to congenital bilateral (both sides) sensorineural hearing loss and goitre with euthyroid or mild hypothyroidism (decreased thyroid gland function).
1884 CE
#13063
Memoir upon the formation of a deaf variety of the human race.
Bell determined that deafness was an inheritable trait and that deaf individuals had a tendency to marry other deaf individuals. As a eugenicist Bell considered this a problem because he thought it risked the developm…
1907 CE
#7226
The dancing mouse: A study in animal behavior.
The first work to examine the characteristics of deaf mice, which became the most important model for the study of genetic deafness. Digital facsimile from the Biodiversity Heritage Library, Internet Archive at this l…
1933 CE
#3206
Zur Pathogenese der Bronchiektasien. I. Mitteilung: Bronchiektasien bei Situs viscerum inversus.
Bronchiectasis and sinus maldevelopment associated with transposition of viscera – “Kartageners syndrome”.