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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 1
1994 1
1995 1
1998 5
1999 1
2000 2
2001 3
2003 2
2004 1
2006 3
2007 3
2009 2
2010 3
2011 2
2012 3
2013 1
2014 3
2015 2
2016 1
2017 1
2018 4
2019 4
2020 3
2021 2
2022 1
2023 1
2024 0

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50 results

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Page 1
The preauricular sinus: a review of its clinical presentation, treatment, and associations.
Scheinfeld NS, Silverberg NB, Weinberg JM, Nozad V. Scheinfeld NS, et al. Pediatr Dermatol. 2004 May-Jun;21(3):191-6. doi: 10.1111/j.0736-8046.2004.21301.x. Pediatr Dermatol. 2004. PMID: 15165194 Review.
Preauricular sinuses are features of other conditions or syndromes in 3-10% of cases, primarily in association with deafness and branchio-oto-renal (BOR) syndrome. When other congenital anomalies coexist with these sinuses, auditory testing and renal u …
Preauricular sinuses are features of other conditions or syndromes in 3-10% of cases, primarily in association with deafness and branchio …
Branchio-oto-renal syndrome.
Kochhar A, Fischer SM, Kimberling WJ, Smith RJ. Kochhar A, et al. Am J Med Genet A. 2007 Jul 15;143A(14):1671-8. doi: 10.1002/ajmg.a.31561. Am J Med Genet A. 2007. PMID: 17238186 Review.
Branchio-oto-renal syndrome, a phenotype consisting of hearing loss, auricular malformations, branchial arch remnants, and renal anomalies is now recognized as one of the more common forms of autosomal dominant syndromic hearing impairment. ...However, …
Branchio-oto-renal syndrome, a phenotype consisting of hearing loss, auricular malformations, branchial arch rem …
Cochlear implantation in Branchiootorenal syndrome - case report and review of the literature.
Tian L, West N, Cayé-Thomasen P. Tian L, et al. Cochlear Implants Int. 2022 Jan;23(1):52-57. doi: 10.1080/14670100.2021.1973209. Epub 2021 Sep 9. Cochlear Implants Int. 2022. PMID: 34498539 Review.
INTRODUCTION: Branchiootorenal syndrome (BOR) manifests with branchial fistulae, otological anomalies and renal dysplasia. ...
INTRODUCTION: Branchiootorenal syndrome (BOR) manifests with branchial fistulae, otological anomalies and renal dysplasia. ...
Branchio-oto-renal syndrome.
Rodríguez Soriano J. Rodríguez Soriano J. J Nephrol. 2003 Jul-Aug;16(4):603-5. J Nephrol. 2003. PMID: 14696767 Review.
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder characterized by the association of branchial cysts or fistulae, external ear malformation and/or preauricular pits, hearing loss and renal anomalies. Mutations in the EYA1 gene, a hum …
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder characterized by the association of branchia …
Microtia and Related Facial Anomalies.
Hartzell LD, Chinnadurai S. Hartzell LD, et al. Clin Perinatol. 2018 Dec;45(4):679-697. doi: 10.1016/j.clp.2018.07.007. Epub 2018 Sep 18. Clin Perinatol. 2018. PMID: 30396412 Review.
Infants may be born with external ear deformities or malformations that can present a diagnostic clue to an affiliated syndrome while also presenting the possibility of surgical intervention. ...
Infants may be born with external ear deformities or malformations that can present a diagnostic clue to an affiliated syndrome while …
From a branchial fistula to a branchiootorenal syndrome: a case report and review of the literature.
Senel E, Kocak H, Akbiyik F, Saylam G, Gulleroglu BN, Senel S. Senel E, et al. J Pediatr Surg. 2009 Mar;44(3):623-5. doi: 10.1016/j.jpedsurg.2008.10.034. J Pediatr Surg. 2009. PMID: 19302870 Review.
Branchial abnormalities constitute 32% to 45% of all neck pathologies in children. They may be a part of branchiootorenal (BOR) syndrome, which is characterized by branchial arch anomalies, preauricular pits, hearing impairment, and renal malformations. ...However, in pati …
Branchial abnormalities constitute 32% to 45% of all neck pathologies in children. They may be a part of branchiootorenal (BOR) syndrome …
Imaging Findings in Syndromes with Temporal Bone Abnormalities.
Ginat DT. Ginat DT. Neuroimaging Clin N Am. 2019 Feb;29(1):117-128. doi: 10.1016/j.nic.2018.08.004. Epub 2018 Oct 29. Neuroimaging Clin N Am. 2019. PMID: 30466636 Review.
This article reviews the imaging features of selected congenital syndromes with temporal bone abnormalities, including Treacher Collins syndrome, oculo-auriculo-vertebral dysplasia spectrum, Klippel-Feil syndrome, branchio-oto-renal syndrome …
This article reviews the imaging features of selected congenital syndromes with temporal bone abnormalities, including Treacher Collins s …
Branchio-oto-renal syndrome.
Smith RJ, Schwartz C. Smith RJ, et al. J Commun Disord. 1998 Sep-Oct;31(5):411-20; quiz 421. doi: 10.1016/s0021-9924(98)00013-6. J Commun Disord. 1998. PMID: 9777487 Review.
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder with branchial, otologic, and renal manifestations. ...
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder with branchial, otologic, and renal manifest …
Using Xenopus to discover new genes involved in branchiootorenal spectrum disorders.
Moody SA, Neilson KM, Kenyon KL, Alfandari D, Pignoni F. Moody SA, et al. Comp Biochem Physiol C Toxicol Pharmacol. 2015 Dec;178:16-24. doi: 10.1016/j.cbpc.2015.06.007. Epub 2015 Jun 24. Comp Biochem Physiol C Toxicol Pharmacol. 2015. PMID: 26117063 Free PMC article. Review.
We discuss the advantages of using this system for gene discovery in a human congenital hearing loss syndrome....
We discuss the advantages of using this system for gene discovery in a human congenital hearing loss syndrome....
[Genetic deafness].
Marcolla A, Bouchetemble P, Lerosey Y, Marie JP, Dehesdin D. Marcolla A, et al. Ann Otolaryngol Chir Cervicofac. 2006 Jun;123(3):143-7. doi: 10.1016/s0003-438x(06)76655-5. Ann Otolaryngol Chir Cervicofac. 2006. PMID: 16840903 Review. French.
RESULTS: Genetic sensorineural syndromic deafness represents 30% of cases of genetic deafness. A frequent cause is Pendred syndrome, which associates congenital sensorineural deafness with goitre and malformations of the inner ear which can be identified on computed tomogr …
RESULTS: Genetic sensorineural syndromic deafness represents 30% of cases of genetic deafness. A frequent cause is Pendred syndrome, …
50 results