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Branchiootorenal Spectrum Disorders

MedGen UID:
432724
Concept ID:
CN043574
Disease or Syndrome
Related genes: SIX5, SIX1, EYA1

Disease characteristics

Excerpted from the GeneReview: Branchiootorenal Spectrum Disorder
Branchiootorenal spectrum disorder (BORSD) is characterized by malformations of the outer, middle, and inner ear associated with conductive, sensorineural, or mixed hearing impairment, branchial fistulae and cysts, and renal malformations ranging from mild renal hypoplasia to bilateral renal agenesis. Some individuals progress to end-stage renal disease (ESRD) later in life. Extreme variability can be observed in the presence, severity, and type of branchial arch, otologic, audiologic, and renal abnormality from right side to left side in an affected individual and also among individuals in the same family. [from GeneReviews]
Authors:
Richard JH Smith   view full author information

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  

Professional guidelines

PubMed

Song MH, Kwon TJ, Kim HR, Jeon JH, Baek JI, Lee WS, Kim UK, Choi JY
PLoS One 2013;8(6):e67236. Epub 2013 Jun 28 doi: 10.1371/journal.pone.0067236. PMID: 23840632Free PMC Article
Kumar S, Deffenbacher K, Cremers CW, Van Camp G, Kimberling WJ
Genet Test 1997-1998;1(4):243-51. doi: 10.1089/gte.1997.1.243. PMID: 10464653

Recent clinical studies

Etiology

Moody SA, Neilson KM, Kenyon KL, Alfandari D, Pignoni F
Comp Biochem Physiol C Toxicol Pharmacol 2015 Dec;178:16-24. Epub 2015 Jun 24 doi: 10.1016/j.cbpc.2015.06.007. PMID: 26117063Free PMC Article

Diagnosis

Moody SA, Neilson KM, Kenyon KL, Alfandari D, Pignoni F
Comp Biochem Physiol C Toxicol Pharmacol 2015 Dec;178:16-24. Epub 2015 Jun 24 doi: 10.1016/j.cbpc.2015.06.007. PMID: 26117063Free PMC Article

Supplemental Content

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