Branchio-oto-renal syndrome

Branchio-oto-renal syndrome
Branchio-oto-renal syndrome
Other names	BOR syndrome, Branchiootorenal syndrome
	Branchio-oto-renal syndrome has an autosomal dominant pattern of inheritance.
Specialty	Medical genetics
Symptoms	Ear abnormalities
Causes	Mutations in genes, EYA1, SIX1, and SIX5
Diagnostic method	Laboratory test results, Physical exam
Treatment	Branchial fistula may need surgery

Branchio-oto-renal syndrome (BOR) is an autosomal dominant genetic disorder involving the kidneys, ears, and neck. It often has also been described as Melnick-Fraser syndrome.^[2]^[3]

Signs and symptoms

The signs and symptoms of branchio-oto-renal syndrome are consistent with underdeveloped (hypoplastic) or absent kidneys with resultant chronic kidney disease or kidney failure. Ear anomalies include extra openings in front of the ears, extra pieces of skin in front of the ears (preauricular tags), or further malformation or absence of the outer ear (pinna). Malformation or absence of the middle ear is also possible, individuals can have mild to profound hearing loss. People with BOR may also have cysts or fistulae along the sides of their neck.^[1] In some individuals and families, renal features are completely absent. The disease may then be termed "branchio-oto syndrome" (BO syndrome).^[4]

Cause

The cause of branchio-oto-renal syndrome are mutations in genes, EYA1, SIX1, and SIX5 (approximately 40 percent of those born with this condition have a mutation in the EYA1 gene).^[1]^[5] Many different abnormalities in these genes have been identified.^{[citation needed]}

Mechanism

The genetics of branchio-oto-renal syndrome indicate it is inherited in an autosomal dominant manner, and results from a mutation in the EYA1 gene.^[6] Autosomal dominant inheritance indicates that the defective gene responsible for a disorder is located on an autosome, and only one copy of the gene is sufficient to cause the disorder, when inherited from a parent who has the disorder. This gene is involved in many facets of embryonic development and is important in the normal formation of many organs and tissues, including the ears, and kidneys before birth.^{[medical citation needed]}

Diagnosis

Diagnosis of BO syndrome or BOR syndrome is clinical, i.e. based on observing an appropriate combination of symptoms.^[4] Only about half of patients have a detectable genetic abnormality, mostly in the EYA1 gene, SIX1 gene or the SIX5 gene.^[4]

Treatment

The treatment of branchio-oto-renal syndrome is done per each affected area (or organ). For example, a person with hearing problems should have appropriate supports and prompt attention for any inflammation of the ear.^[4]^[7]

A specialist should observe any kidney problems. Surgical repair may be needed depending on the degree of a defect or problem, whether a transplant or dialysis is needed.^[8]

Epidemiology

The epidemiology of branchio-oto-renal syndrome has it with a prevalence of 1/40,000 in Western countries. A 2014 review found 250 such cases in the country of Japan.^[9]

References

^ ^a ^b ^c "Branchio Oto Renal Syndrome - NORD (National Organization for Rare Disorders)". NORD (National Organization for Rare Disorders). Retrieved 2015-11-29.
^ ^a ^b "Branchiootorenal syndrome". Genetics Home Reference. 2015-11-23. Archived from the original on 2016-02-29. Retrieved 2015-11-29.
^ ^a ^b ^c "Branchiootorenal syndrome | Disease | Overview | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 2015-11-29.
^ ^a ^b ^c ^d Smith, Richard J.H. (1993-01-01). "Branchiootorenal Spectrum Disorder". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). Branchiootorenal Spectrum Disorders. Seattle (WA): University of Washington, Seattle. PMID 20301554.|updated, 2015|
^ Little, Melissa Helen (2015-08-06). Kidney Development, Disease, Repair and Regeneration. Academic Press. p. 269. ISBN 9780128004388.
^ Online Mendelian Inheritance in Man (OMIM): Branchiootorenal Syndrome 1; BOR1 - 113650
^ Niparko, John K. (2009-01-01). Cochlear Implants: Principles & Practices. Lippincott Williams & Wilkins. p. 53. ISBN 9780781777490.
^ Izzedine, Hassane; Tankere, Frederic; Launay-Vacher, Vincent; Deray, Gilbert (2004-02-01). "Ear and kidney syndromes: Molecular versus clinical approach". Kidney International. 65 (2): 369–385. doi:10.1111/j.1523-1755.2004.00390.x. ISSN 0085-2538. PMID 14717907.
^ Morisada, Naoya; Nozu, Kandai; Iijima, Kazumoto (2014-06-01). "Branchio-oto-renal syndrome: Comprehensive review based on nationwide surveillance in Japan". Pediatrics International. 56 (3): 309–314. doi:10.1111/ped.12357. ISSN 1442-200X. PMID 24730701. S2CID 40930806.

External links

Scholia has a topic profile for Branchio-oto-renal syndrome.

[gene-1] "Branchio Oto Renal Syndrome - NORD (National Organization for Rare Disorders)". NORD (National Organization for Rare Disorders). Retrieved 2015-11-29.

[genh-2] "Branchiootorenal syndrome". Genetics Home Reference. 2015-11-23. Archived from the original on 2016-02-29. Retrieved 2015-11-29.

[gar-3] "Branchiootorenal syndrome | Disease | Overview | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 2015-11-29.

[Smith-4] Smith, Richard J.H. (1993-01-01). "Branchiootorenal Spectrum Disorder". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). Branchiootorenal Spectrum Disorders. Seattle (WA): University of Washington, Seattle. PMID 20301554.|updated, 2015|

[5] Little, Melissa Helen (2015-08-06). Kidney Development, Disease, Repair and Regeneration. Academic Press. p. 269. ISBN 9780128004388.

[6] Online Mendelian Inheritance in Man (OMIM): Branchiootorenal Syndrome 1; BOR1 - 113650

[7] Niparko, John K. (2009-01-01). Cochlear Implants: Principles & Practices. Lippincott Williams & Wilkins. p. 53. ISBN 9780781777490.

[8] Izzedine, Hassane; Tankere, Frederic; Launay-Vacher, Vincent; Deray, Gilbert (2004-02-01). "Ear and kidney syndromes: Molecular versus clinical approach". Kidney International. 65 (2): 369–385. doi:10.1111/j.1523-1755.2004.00390.x. ISSN 0085-2538. PMID 14717907.

[9] Morisada, Naoya; Nozu, Kandai; Iijima, Kazumoto (2014-06-01). "Branchio-oto-renal syndrome: Comprehensive review based on nationwide surveillance in Japan". Pediatrics International. 56 (3): 309–314. doi:10.1111/ped.12357. ISSN 1442-200X. PMID 24730701. S2CID 40930806.

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