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Quoted phrase not found in phrase index: "Hearing loss, autosomal dominant 79"
Page 1
Cochlear implantation outcomes in children with Waardenburg syndrome.
Amirsalari S, Ajallouyean M, Saburi A, Haddadi Fard A, Abed M, Ghazavi Y. Amirsalari S, et al. Eur Arch Otorhinolaryngol. 2012 Oct;269(10):2179-83. doi: 10.1007/s00405-011-1877-3. Epub 2011 Dec 11. Eur Arch Otorhinolaryngol. 2012. PMID: 22159916
Waardenburg syndrome (WS) is an autosomal dominant disease, characterized by dystopia canthorum, hyperplasia of the eyebrows, heterochromia iridis, white forelock, and congenital sensori-neural hearing loss (SNHL). ...There was a significant difference …
Waardenburg syndrome (WS) is an autosomal dominant disease, characterized by dystopia canthorum, hyperplasia of the eyebrows, …
On-Top Index Pollicization After a Partial Amputation of a Syndactylized Hypoplastic Thumb in a Patient With Townes-Brocks Syndrome.
Lorencin M, Bulic K. Lorencin M, et al. Ann Plast Surg. 2017 Sep;79(3):e7-e10. doi: 10.1097/SAP.0000000000001080. Ann Plast Surg. 2017. PMID: 28509696
Townes-Brocks syndrome is a rare autosomal dominant syndrome characterized by multiple malformations, including thumb anomalies. ...
Townes-Brocks syndrome is a rare autosomal dominant syndrome characterized by multiple malformations, including thumb anomalie …
Otosclerosis in a black child: diagnostic acoustic impedance studies.
Schweitzer VG, Lilly DJ. Schweitzer VG, et al. Int J Pediatr Otorhinolaryngol. 1984 Oct;8(1):79-90. doi: 10.1016/s0165-5876(84)80028-2. Int J Pediatr Otorhinolaryngol. 1984. PMID: 6500827
Otosclerosis classically describes an osteodystrophic change in the bony labyrinth and stapes footplate, of autosomal dominant inheritance, reported rare under the age of 5, extremely "rare" in the Oriental and Black race, "non-existent" in the American Indian, and …
Otosclerosis classically describes an osteodystrophic change in the bony labyrinth and stapes footplate, of autosomal dominant …