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Bardet-Biedl syndrome(BBS)

MedGen UID:
156019
Concept ID:
C0752166
Disease or Syndrome
Synonym: BBS
SNOMED CT: Bardet-Biedl syndrome (5619004); LMBB - Laurence-Moon-Bardet-Biedl syndrome (5619004); Biedl-Bardet syndrome (5619004)
Modes of inheritance:
Autosomal recessive inheritance
MedGen UID:
141025
Concept ID:
C0441748
Intellectual Product
Source: Orphanet
A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele).
Oligogenic inheritance
MedGen UID:
253949
Concept ID:
C1136026
Genetic Function
Source: Orphanet
A type of multifactorial inheritance governed by the simultaneous action of a few gene loci. It is recommended this term be used for traits governed by three loci, although it is noted that usage of this term in the literature is not uniform.
 
Genes (locations): BBS1 (11q13.2); BBS4 (15q24.1); MKKS (20p12.2); SDCCAG8 (1q43-44)
Related genes: BBS12, BBS5, TTC8, TMEM67, ARL6, CEP290, BBS10, CCDC28B, BBS7, MKS1, WDPCP, BBS9, TRIM32, BBS2
 
Monarch Initiative: MONDO:0015229
OMIM® Phenotypic series: PS209900
Orphanet: ORPHA110

Definition

Bardet-Biedl syndrome is a disorder that affects many parts of the body. The signs and symptoms of this condition vary among affected individuals, even among members of the same family.

Vision loss is one of the major features of Bardet-Biedl syndrome. Loss of vision occurs as the light-sensing tissue at the back of the eye (the retina) gradually deteriorates. Problems with night vision become apparent by mid-childhood, followed by blind spots that develop in the side (peripheral) vision. Over time, these blind spots enlarge and merge to produce tunnel vision. Most people with Bardet-Biedl syndrome also develop blurred central vision (poor visual acuity) and become legally blind by adolescence or early adulthood.

Obesity is another characteristic feature of Bardet-Biedl syndrome. Abnormal weight gain typically begins in early childhood and continues to be an issue throughout life. Complications of obesity can include type 2 diabetes, high blood pressure (hypertension), and abnormally high cholesterol levels (hypercholesterolemia).

Other major signs and symptoms of Bardet-Biedl syndrome include the presence of extra fingers or toes (polydactyly), intellectual disability or learning problems, and abnormalities of the genitalia. Most affected males produce reduced amounts of sex hormones (hypogonadism), and they are usually unable to father biological children (infertile). Many people with Bardet-Biedl syndrome also have kidney abnormalities, which can be serious or life-threatening.

Additional features of Bardet-Biedl syndrome can include impaired speech, delayed development of motor skills such as standing and walking, behavioral problems such as emotional immaturity and inappropriate outbursts, and clumsiness or poor coordination. Distinctive facial features, dental abnormalities, unusually short or fused fingers or toes, and a partial or complete loss of the sense of smell (anosmia) have also been reported in some people with Bardet-Biedl syndrome. Additionally, this condition can affect the heart, liver, and digestive system. [from MedlinePlus Genetics]

Professional guidelines

PubMed

Han JC, Rasmussen MC, Forte AR, Schrage SB, Zafar SK, Haqq AM
Gastroenterol Clin North Am 2023 Dec;52(4):733-750. Epub 2023 Sep 27 doi: 10.1016/j.gtc.2023.08.005. PMID: 37919024
Spahiu L, Behluli E, Grajçevci-Uka V, Liehr T, Temaj G
J Mother Child 2022 Mar 1;26(1):118-123. Epub 2023 Feb 22 doi: 10.34763/jmotherandchild.20222601.d-22-00034. PMID: 36803942Free PMC Article
Raina R, Chakraborty R, Sethi SK, Kumar D, Gibson K, Bergmann C
Am J Kidney Dis 2021 Jul;78(1):125-141. Epub 2021 Jan 6 doi: 10.1053/j.ajkd.2020.10.021. PMID: 33418012

Curated

Slavotinek A, Beales P
Eur J Hum Genet 2011 Mar;19(3) Epub 2010 Dec 8 doi: 10.1038/ejhg.2010.199. PMID: 21150877Free PMC Article

Recent clinical studies

Etiology

Haqq AM, Chung WK, Dollfus H, Haws RM, Martos-Moreno GÁ, Poitou C, Yanovski JA, Mittleman RS, Yuan G, Forsythe E, Clément K, Argente J
Lancet Diabetes Endocrinol 2022 Dec;10(12):859-868. Epub 2022 Nov 7 doi: 10.1016/S2213-8587(22)00277-7. PMID: 36356613Free PMC Article
McConnachie DJ, Stow JL, Mallett AJ
Am J Kidney Dis 2021 Mar;77(3):410-419. Epub 2020 Oct 9 doi: 10.1053/j.ajkd.2020.08.012. PMID: 33039432
Littleton SH, Berkowitz RI, Grant SFA
Mol Diagn Ther 2020 Dec;24(6):653-663. Epub 2020 Oct 1 doi: 10.1007/s40291-020-00496-1. PMID: 33006084Free PMC Article
Kostovski M, Tasic V, Laban N, Polenakovic M, Danilovski D, Gucev Z
Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2017 Dec 1;38(3):121-133. doi: 10.2478/prilozi-2018-0013. PMID: 29668472
Forsythe E, Beales PL
Eur J Hum Genet 2013 Jan;21(1):8-13. Epub 2012 Jun 20 doi: 10.1038/ejhg.2012.115. PMID: 22713813Free PMC Article

Diagnosis

Spahiu L, Behluli E, Grajçevci-Uka V, Liehr T, Temaj G
J Mother Child 2022 Mar 1;26(1):118-123. Epub 2023 Feb 22 doi: 10.34763/jmotherandchild.20222601.d-22-00034. PMID: 36803942Free PMC Article
Haqq AM, Chung WK, Dollfus H, Haws RM, Martos-Moreno GÁ, Poitou C, Yanovski JA, Mittleman RS, Yuan G, Forsythe E, Clément K, Argente J
Lancet Diabetes Endocrinol 2022 Dec;10(12):859-868. Epub 2022 Nov 7 doi: 10.1016/S2213-8587(22)00277-7. PMID: 36356613Free PMC Article
Raina R, Chakraborty R, Sethi SK, Kumar D, Gibson K, Bergmann C
Am J Kidney Dis 2021 Jul;78(1):125-141. Epub 2021 Jan 6 doi: 10.1053/j.ajkd.2020.10.021. PMID: 33418012
Dan H, Huang X, Xing Y, Shen Y
Mol Genet Genomic Med 2020 Mar;8(3):e1131. Epub 2020 Jan 20 doi: 10.1002/mgg3.1131. PMID: 31960602Free PMC Article
Forsythe E, Beales PL
Eur J Hum Genet 2013 Jan;21(1):8-13. Epub 2012 Jun 20 doi: 10.1038/ejhg.2012.115. PMID: 22713813Free PMC Article

Therapy

Feig DS, Sanchez JJ, Murphy KE, Asztalos E, Zinman B, Simmons D, Haqq AM, Fantus IG, Lipscombe L, Armson A, Barrett J, Donovan L, Karanicolas P, Tobin S, Mangoff K, Klein G, Jiang Y, Tomlinson G, Hamilton J; MiTy Kids Collaborative Group
Lancet Diabetes Endocrinol 2023 Mar;11(3):191-202. Epub 2023 Feb 3 doi: 10.1016/S2213-8587(23)00004-9. PMID: 36746160
Forsythe E, Haws RM, Argente J, Beales P, Martos-Moreno GÁ, Dollfus H, Chirila C, Gnanasakthy A, Buckley BC, Mallya UG, Clément K, Haqq AM
Orphanet J Rare Dis 2023 Jan 16;18(1):12. doi: 10.1186/s13023-022-02602-4. PMID: 36647077Free PMC Article
Haqq AM, Chung WK, Dollfus H, Haws RM, Martos-Moreno GÁ, Poitou C, Yanovski JA, Mittleman RS, Yuan G, Forsythe E, Clément K, Argente J
Lancet Diabetes Endocrinol 2022 Dec;10(12):859-868. Epub 2022 Nov 7 doi: 10.1016/S2213-8587(22)00277-7. PMID: 36356613Free PMC Article
Olson AJ, Krentz AD, Finta KM, Okorie UC, Haws RM
J Pediatr 2019 Jan;204:31-37. Epub 2018 Oct 4 doi: 10.1016/j.jpeds.2018.08.068. PMID: 30293640
Yeung JC, Katwa UA, Lee GS
Int J Pediatr Otorhinolaryngol 2017 Nov;102:127-132. Epub 2017 Sep 12 doi: 10.1016/j.ijporl.2017.09.004. PMID: 29106859

Prognosis

De Groof J, Dachy A, Breysem L, Mekahli D
Arch Pediatr 2023 May;30(4):240-246. Epub 2023 Apr 14 doi: 10.1016/j.arcped.2023.02.005. PMID: 37062654
Feig DS, Sanchez JJ, Murphy KE, Asztalos E, Zinman B, Simmons D, Haqq AM, Fantus IG, Lipscombe L, Armson A, Barrett J, Donovan L, Karanicolas P, Tobin S, Mangoff K, Klein G, Jiang Y, Tomlinson G, Hamilton J; MiTy Kids Collaborative Group
Lancet Diabetes Endocrinol 2023 Mar;11(3):191-202. Epub 2023 Feb 3 doi: 10.1016/S2213-8587(23)00004-9. PMID: 36746160
Gupta N, D'Acierno M, Zona E, Capasso G, Zacchia M
Am J Med Genet C Semin Med Genet 2022 Mar;190(1):9-19. Epub 2022 Apr 4 doi: 10.1002/ajmg.c.31970. PMID: 35373910Free PMC Article
Adamiok-Ostrowska A, Piekiełko-Witkowska A
Cells 2020 Apr 8;9(4) doi: 10.3390/cells9040907. PMID: 32276433Free PMC Article
Kostovski M, Tasic V, Laban N, Polenakovic M, Danilovski D, Gucev Z
Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2017 Dec 1;38(3):121-133. doi: 10.2478/prilozi-2018-0013. PMID: 29668472

Clinical prediction guides

Forsythe E, Mallya UG, Yang M, Huber C, Cala ML, Greatsinger A, Hagopian E, Pomeroy J, Haqq AM
Orphanet J Rare Dis 2023 Jul 7;18(1):182. doi: 10.1186/s13023-023-02723-4. PMID: 37415189Free PMC Article
Feig DS, Sanchez JJ, Murphy KE, Asztalos E, Zinman B, Simmons D, Haqq AM, Fantus IG, Lipscombe L, Armson A, Barrett J, Donovan L, Karanicolas P, Tobin S, Mangoff K, Klein G, Jiang Y, Tomlinson G, Hamilton J; MiTy Kids Collaborative Group
Lancet Diabetes Endocrinol 2023 Mar;11(3):191-202. Epub 2023 Feb 3 doi: 10.1016/S2213-8587(23)00004-9. PMID: 36746160
Gupta N, D'Acierno M, Zona E, Capasso G, Zacchia M
Am J Med Genet C Semin Med Genet 2022 Mar;190(1):9-19. Epub 2022 Apr 4 doi: 10.1002/ajmg.c.31970. PMID: 35373910Free PMC Article
Chandrasekar SP, Namboothiri S, Sen P, Sarangapani S
Indian J Med Res 2018 Feb;147(2):177-182. doi: 10.4103/ijmr.IJMR_1822_15. PMID: 29806606Free PMC Article
Forsythe E, Beales PL
Eur J Hum Genet 2013 Jan;21(1):8-13. Epub 2012 Jun 20 doi: 10.1038/ejhg.2012.115. PMID: 22713813Free PMC Article

Recent systematic reviews

Sonner S, Reilly K, Woolf AS, Chandler N, Kilby MD, Maher ER, Flanagan C, McKnight AJ, Mone F
Prenat Diagn 2024 Feb;44(2):187-195. Epub 2023 Dec 6 doi: 10.1002/pd.6479. PMID: 38056891
Deng L, Liu Y, Yuan M, Meng M, Yang Y, Sun L
Clin Chim Acta 2022 Mar 1;528:16-28. Epub 2022 Jan 20 doi: 10.1016/j.cca.2022.01.012. PMID: 35065907

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