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Monogenic and Syndromic Causes of Obesity

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Management of Prader-Willi Syndrome
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Abstract

Obesity is a pediatric and adult global health problem of epidemic proportions in westernized societies. It results from imbalance of energy intake and expenditure. The cause of obesity is heterogeneous with complex biological processes playing a role including control of peptides involved in regulating appetite, cellular energy and metabolism, and fat production influenced by environmental interactions. Advances in genetic technology have led to discoveries of single gene and copy number variants playing a role in early onset of severe obesity and other obesity phenotypes. Heritability studies have shown that genetic components can contribute to 40–70% of obesity with over 350 potential genes reported in the literature. Monogenic causes of obesity and dozens of syndromic examples are discussed such as Prader-Willi syndrome, in which individuals develop obesity due to hyperphagia and decreased resting energy expenditure. The current knowledge of monogenic and syndromic causes of obesity, their genotype, and clinical features are summarized with descriptions. The genetic dissection of obesity with characterization of biological pathways and gene-protein environmental interactions at the brain level will contribute to understanding disease mechanisms and outcomes. This information can be applied for early diagnosis, prevention, and treatment as well as elucidating therapeutic targets for development of personalized medicines designed for obesity in humans.

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References

  1. Friedman JM. Modern science versus the stigma of obesity. Nat Med. 2004;10(6):563–9.

    Article  CAS  PubMed  Google Scholar 

  2. Kelly T, Yang W, Chen C-S, Reynolds K, He J. Global burden of obesity in 2005 and projections to 2030. Int J Obes. 2008;32(9):1431–7.

    Article  CAS  Google Scholar 

  3. de Onis M, Blössner M, Borghi E. Global prevalence and trends of overweight and obesity among preschool children. Am J Clin Nutr. 2010;92(5):1257–64.

    Article  PubMed  Google Scholar 

  4. Finucane MM, Stevens GA, Cowan MJ, Danaei G, Lin JK, Paciorek CJ, et al. National, regional, and global trends in body-mass index since 1980: systematic analysis of health examination surveys and epidemiological studies with 960 country-years and 9·1 million participants. Lancet Lond Engl. 2011;377(9765):557–67.

    Article  Google Scholar 

  5. Yanovski SZ, Yanovski JA. Obesity prevalence in the United States--up, down, or sideways? N Engl J Med. 2011;364(11):987–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Daniels SR, Arnett DK, Eckel RH, Gidding SS, Hayman LL, Kumanyika S, et al. Overweight in children and adolescents: pathophysiology, consequences, prevention, and treatment. Circulation. 2005;111(15):1999–2012.

    Article  PubMed  Google Scholar 

  7. Silber SJ, Barbey N. Scientific molecular basis for treatment of reproductive failure in the human: an insight into the future. Biochim Biophys Acta. 2012;1822(12):1981–96.

    Article  CAS  PubMed  Google Scholar 

  8. Hruby A, Hu FB. The epidemiology of obesity: a big picture. PharmacoEconomics. 2015;33(7):673–89.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Choquet H, Meyre D. Genetics of obesity: what have we learned? Curr Genomics. 2011;12(3):169–79.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Cummings DE, Schwartz MW. Genetics and pathophysiology of human obesity. Annu Rev Med. 2003;54:453–71.

    Article  CAS  PubMed  Google Scholar 

  11. Wardle J, Carnell S, Haworth CM, Plomin R. Evidence for a strong genetic influence on childhood adiposity despite the force of the obesogenic environment. Am J Clin Nutr. 2008;87(2):398–404.

    Article  CAS  PubMed  Google Scholar 

  12. Locke AE, Kahali B, Berndt SI, Justice AE, Pers TH, Day FR, et al. Genetic studies of body mass index yield new insights for obesity biology. Nature. 2015;518(7538):197–206.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Chiurazzi M, Cozzolino M, Orsini RC, Di Maro M, Di Minno MND, Colantuoni A. Impact of genetic variations and epigenetic mechanisms on the risk of obesity. Int J Mol Sci. 2020;21(23)

    Google Scholar 

  14. Butler MG, Wang K, Marshall JD, Naggert JK, Rethmeyer JA, Gunewardena SS, et al. Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes. Adv Genomics Genet. 2015;2015(5):53–75.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Stunkard AJ, Harris JR, Pedersen NL, McClearn GE. The body-mass index of twins who have been reared apart. N Engl J Med. 1990;322(21):1483–7.

    Article  CAS  PubMed  Google Scholar 

  16. Lajunen H-R, Kaprio J, Keski-Rahkonen A, Rose RJ, Pulkkinen L, Rissanen A, et al. Genetic and environmental effects on body mass index during adolescence: a prospective study among Finnish twins. Int J Obes. 2009;33(5):559–67.

    Article  Google Scholar 

  17. Butler MG, McGuire A, Manzardo AM. Clinically relevant known and candidate genes for obesity and their overlap with human infertility and reproduction. J Assist Reprod Genet. 2015;32(4):495–508.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Wright AF, Carothers AD, Campbell H. Gene-environment interactions–the BioBank UK study. Pharmacogenomics J. 2002;2(2):75–82.

    Article  CAS  PubMed  Google Scholar 

  19. Kaur Y, de Souza RJ, Gibson WT, Meyre D. A systematic review of genetic syndromes with obesity. Obes Rev. 2017;18(6):603–34.

    Article  CAS  PubMed  Google Scholar 

  20. Scherag A, Dina C, Hinney A, Vatin V, Scherag S, Vogel CIG, et al. Two new loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups. PLoS Genet. 2010;6(4):e1000916.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Rankinen T, Zuberi A, Chagnon YC, Weisnagel SJ, Argyropoulos G, Walts B, et al. The human obesity gene map: the 2005 update. Obes Silver Spring MD. 2006;14(4):529–644.

    Article  Google Scholar 

  22. Frayling TM, Timpson NJ, Weedon MN, Zeggini E, Freathy RM, Lindgren CM, et al. A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Science. 2007;316(5826):889–94.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Dina C, Meyre D, Gallina S, Durand E, Körner A, Jacobson P, et al. Variation in FTO contributes to childhood obesity and severe adult obesity. Nat Genet. 2007;39(6):724–6.

    Article  CAS  PubMed  Google Scholar 

  24. Hinney A, Nguyen TT, Scherag A, Friedel S, Brönner G, Müller TD, et al. Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants. PLoS One. 2007;2(12):e1361.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, et al. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet. 2010;42(11):937–48.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Geller F, Reichwald K, Dempfle A, Illig T, Vollmert C, Herpertz S, et al. Melanocortin-4 receptor gene variant I103 is negatively associated with obesity. Am J Hum Genet. 2004;74(3):572–81.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Stutzmann F, Vatin V, Cauchi S, Morandi A, Jouret B, Landt O, et al. Non-synonymous polymorphisms in melanocortin-4 receptor protect against obesity: the two facets of a Janus obesity gene. Hum Mol Genet. 2007;16(15):1837–44.

    Article  CAS  PubMed  Google Scholar 

  28. Bittel DC, Kibiryeva N, Dasouki M, Knoll JHM, Butler MG. A 9-year-old male with a duplication of chromosome 3p25.3p26.2: clinical report and gene expression analysis. Am J Med Genet A. 2006;140(6):573–9.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Choquet H, Meyre D. Molecular basis of obesity: current status and future prospects. Curr Genomics. 2011;12(3):154–68.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Farooqi IS, O’Rahilly S. Monogenic obesity in humans. Annu Rev Med. 2005;56:443–58.

    Article  CAS  PubMed  Google Scholar 

  31. Butler MG. Single gene and Syndromic causes of obesity: illustrative examples. Prog Mol Biol Transl Sci. 2016;140:1–45.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Klok MD, Jakobsdottir S, Drent ML. The role of leptin and ghrelin in the regulation of food intake and body weight in humans: a review. Obes Rev. 2007;8(1):21–34.

    Article  CAS  PubMed  Google Scholar 

  33. Perry B, Wang Y. Appetite regulation and weight control: the role of gut hormones. Nutr Diabetes. 2012;2:e26.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Pigeyre M, Yazdi FT, Kaur Y, Meyre D. Recent progress in genetics, epigenetics and metagenomics unveils the pathophysiology of human obesity. Clin Sci Lond Engl 1979. 2016;130(12):943–86.

    CAS  Google Scholar 

  35. Krude H, Biebermann H, Luck W, Horn R, Brabant G, Grüters A. Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans. Nat Genet. 1998;19(2):155–7.

    Article  CAS  PubMed  Google Scholar 

  36. Creemers JWM, Lee YS, Oliver RL, Bahceci M, Tuzcu A, Gokalp D, et al. Mutations in the amino-terminal region of proopiomelanocortin (POMC) in patients with early-onset obesity impair POMC sorting to the regulated secretory pathway. J Clin Endocrinol Metab. 2008;93(11):4494–9.

    Article  CAS  PubMed  Google Scholar 

  37. Clément K, Vaisse C, Lahlou N, Cabrol S, Pelloux V, Cassuto D, et al. A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction. Nature. 1998;392(6674):398–401.

    Article  PubMed  Google Scholar 

  38. Millington GW. The role of proopiomelanocortin (POMC) neurones in feeding behaviour. Nutr Metab. 2007;4:18.

    Article  Google Scholar 

  39. Farooqi IS, Volders K, Stanhope R, Heuschkel R, White A, Lank E, et al. Hyperphagia and early-onset obesity due to a novel homozygous missense mutation in prohormone convertase 1/3. J Clin Endocrinol Metab. 2007;92(9):3369–73.

    Article  CAS  PubMed  Google Scholar 

  40. Burnett LC, LeDuc CA, Sulsona CR, Paull D, Rausch R, Eddiry S, et al. Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome. J Clin Invest. 2017;127(1):293–305.

    Article  PubMed  Google Scholar 

  41. Dasouki MJ, Youngs EL, Hovanes K. Structural chromosome abnormalities associated with obesity: report of four new subjects and review of literature. Curr Genomics. 2011;12(3):190–203.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Xia Q, Grant SFA. The genetics of human obesity. Ann N Y Acad Sci. 2013;1281:178–90.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Bell CG, Walley AJ, Froguel P. The genetics of human obesity. Nat Rev Genet. 2005;6(3):221–34.

    Article  CAS  PubMed  Google Scholar 

  44. Montague CT, Farooqi IS, Whitehead JP, Soos MA, Rau H, Wareham NJ, et al. Congenital leptin deficiency is associated with severe early-onset obesity in humans. Nature. 1997;387(6636):903–8.

    Article  CAS  PubMed  Google Scholar 

  45. Farooqi S, O’Rahilly S. Genetics of obesity in humans. Endocr Rev. 2006;27(7):710–8.

    Article  CAS  PubMed  Google Scholar 

  46. Chambers JC, Elliott P, Zabaneh D, Zhang W, Li Y, Froguel P, et al. Common genetic variation near MC4R is associated with waist circumference and insulin resistance. Nat Genet. 2008;40(6):716–8.

    Article  CAS  PubMed  Google Scholar 

  47. Scuteri A, Sanna S, Chen W-M, Uda M, Albai G, Strait J, et al. Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. PLoS Genet. 2007;3(7):e115.

    Article  PubMed  PubMed Central  Google Scholar 

  48. Krashes MJ, Lowell BB, Garfield AS. Melanocortin-4 receptor-regulated energy homeostasis. Nat Neurosci. 2016;19(2):206–19.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Sangu N, Shimojima K, Shimada S, Ando T, Yamamoto T. Growth patterns of patients with 1p36 deletion syndrome. Congenit Anom. 2014;54(2):82–6.

    Article  CAS  Google Scholar 

  50. Walters-Sen LC, Windemuth K, Angione K, Nandhlal J, Milunsky JM. Familial transmission of 5p13.2 duplication due to maternal der(X)ins(X;5). Eur J Med Genet. 2015;58(5):305–9.

    Article  PubMed  Google Scholar 

  51. Bonaglia MC, Ciccone R, Gimelli G, Gimelli S, Marelli S, Verheij J, et al. Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotype. Eur J Hum Genet. 2008;16(12):1443–9.

    Article  CAS  PubMed  Google Scholar 

  52. Miller DT, Chung W, Nasir R, Shen Y, Steinman KJ, Wu B-L, et al. 16p11.2 Recurrent Microdeletion. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al., editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993 [cited 2021 Feb 1]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK11167/.

  53. Bertapelli F, Pitetti K, Agiovlasitis S, Guerra-Junior G. Overweight and obesity in children and adolescents with Down syndrome-prevalence, determinants, consequences, and interventions: a literature review. Res Dev Disabil. 2016;57:181–92.

    Article  PubMed  Google Scholar 

  54. Lebenthal Y, Levy S, Sofrin-Drucker E, Nagelberg N, Weintrob N, Shalitin S, et al. The natural history of metabolic comorbidities in turner syndrome from childhood to early adulthood: comparison between 45,X monosomy and other karyotypes. Front Endocrinol. 2018;9:27.

    Article  Google Scholar 

  55. Bojesen A, Kristensen K, Birkebaek NH, Fedder J, Mosekilde L, Bennett P, et al. The metabolic syndrome is frequent in Klinefelter’s syndrome and is associated with abdominal obesity and hypogonadism. Diabetes Care. 2006;29(7):1591–8.

    Article  PubMed  Google Scholar 

  56. Paisey RB, Steeds R, Barrett T, Williams D, Geberhiwot T, Gunay-Aygun M. Alström Syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al., editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993 [cited 2021 Feb 1]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1267/.

  57. Marshall JD, Maffei P, Collin GB, Naggert JK. Alström syndrome: genetics and clinical overview. Curr Genomics. 2011;12(3):225–35.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Forsyth R, Gunay-Aygun M. Bardet-Biedl Syndrome Overview. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al., editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993 [cited 2021 Feb 1]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1363/.

  59. Lower KM, Turner G, Kerr BA, Mathews KD, Shaw MA, Gedeon AK, et al. Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome. Nat Genet. 2002;32(4):661–5.

    Article  CAS  PubMed  Google Scholar 

  60. Bellad A, Bandari AK, Pandey A, Girimaji SC, Muthusamy B. A novel missense variant in PHF6 gene causing Börjeson-Forssman-Lehman syndrome. J Mol Neurosci. 2020;70(9):1403–9.

    Article  CAS  PubMed  Google Scholar 

  61. Hidestrand P, Vasconez H, Cottrill C. Carpenter syndrome. J Craniofac Surg. 2009;20(1):254–6.

    Article  PubMed  Google Scholar 

  62. Raible SE, Mehta D, Bettale C, Fiordaliso S, Kaur M, Medne L, et al. Clinical and molecular spectrum of CHOPS syndrome. Am J Med Genet A. 2019;179(7):1126–38.

    CAS  PubMed  PubMed Central  Google Scholar 

  63. Abidi FE, Cardoso C, Lossi A-M, Lowry RB, Depetris D, Mattéi M-G, et al. Mutation in the 5′ alternatively spliced region of the XNP/ATR-X gene causes Chudley-Lowry syndrome. Eur J Hum Genet. 2005;13(2):176–83.

    Article  CAS  PubMed  Google Scholar 

  64. Rogers RC, Abidi FE. Coffin-Lowry Syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al., editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993 [cited 2021 Feb 1]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1346/.

  65. Wang H, Falk MJ, Wensel C, Traboulsi EI. Cohen Syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al., editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993 [cited 2021 Feb 1]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1482/.

  66. Deardorff MA, Noon SE, Krantz ID. Cornelia de Lange Syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al., editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993 [cited 2021 Feb 1]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1104/.

  67. Mariani M, Decimi V, Bettini LR, Maitz S, Gervasini C, Masciadri M, et al. Adolescents and adults affected by Cornelia de Lange syndrome: a report of 73 Italian patients. Am J Med Genet C Semin Med Genet. 2016;172(2):206–13.

    Article  PubMed  Google Scholar 

  68. Haldeman-Englert CR, Hurst AC, Levine MA. Disorders of GNAS Inactivation. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al., editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993 [cited 2021 Feb 1]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK459117/.

  69. Butler MG. Imprinting disorders in humans: a review. Curr Opin Pediatr. 2020;32(6):719–29.

    Article  PubMed  PubMed Central  Google Scholar 

  70. Hunter JE, Berry-Kravis E, Hipp H, Todd PK. FMR1 Disorders. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al., editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993 [cited 2021 Feb 1]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1384/.

  71. McLennan Y, Polussa J, Tassone F, Hagerman R. Fragile X syndrome. Curr Genomics. 2011;12(3):216–24.

    Google Scholar 

  72. Baumbach L, Schiavi A, Bartlett R, Perera E, Day J, Brown MR, et al. Clinical, biochemical, and molecular investigations of a genetic isolate of growth hormone insensitivity (Laron's syndrome). Clin Endocrinol Metab. 1997;82(2):444–51.

    CAS  Google Scholar 

  73. Adam MP, Hudgins L, Hannibal M. Kabuki Syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al., editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993 [cited 2021 Feb 1]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK62111/.

  74. Dodé C, Teixeira L, Levilliers J, Fouveaut C, Bouchard P, Kottler M-L, et al. Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2. PLoS Genet. 2006;2(10):e175.

    Article  PubMed  PubMed Central  Google Scholar 

  75. Dodé C, Hardelin J-P. Kallmann syndrome. Eur J Hum Genet. 2009;17(2):139–46.

    Article  PubMed  Google Scholar 

  76. Kleefstra T, de Leeuw N. Kleefstra Syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al. editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993. [cited 2021 Feb 1]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK47079/.

  77. Williemsen MH, Vulto-van Silfhout AT, Nillesen WM, Wissink-Lindhout WM, van Bokhoven H, Philip N, et al. Update on Kleefstra syndrome. Mol Syndromol. 2012;2(3–5):202–12.

    Google Scholar 

  78. Di Donato N, Riess A, Hackmann K, Rump A, Huebner A, von der Hagen M, et al. Macrocephaly, obesity, mental (intellectual) disability, and ocular abnormalities: alternative definition and further delineation of MOMO syndrome. Am J Med Genet A. 2012;158A(11):2857–62.

    Article  PubMed  Google Scholar 

  79. Hampshire DJ, Ayub M, Springell K, Roberts E, Jafri H, Rashid Y, et al. MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34. Eur J Hum Genet. 2006;14(5):543–8.

    Article  CAS  PubMed  Google Scholar 

  80. Angulo MA, Butler MG, Cataletto ME. Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings. J Endocrinol Investig. 2015;38(12):1249–63.

    Article  CAS  Google Scholar 

  81. Driscoll DJ, Miller JL, Schwartz S, Cassidy SB. Prader-Willi Syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al., editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993 [cited 2021 Feb 1]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1330/.

  82. Butler MG, Hartin SN, Hossain WA, Manzardo AM, Kimonis V, Dykens E, et al. Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study. J Med Genet. 2019;56(3):149–53.

    Article  CAS  PubMed  Google Scholar 

  83. Stevens CA. Rubinstein-Taybi Syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al., editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993 [cited 2021 Feb 1]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1526/,

  84. Smith AC, Boyd KE, Brennan C, Charles J, Elsea SH, Finucane BM, et al. Smith-Magenis Syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, et al., editors. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993 [cited 2021 Feb 3]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1310/.

  85. Rodríguez-López R, Pérez JMC, Balsera AM, Rodríguez GG, Moreno TH, García de Cáceres M, et al. The modifier effect of the BDNF gene in the phenotype of the WAGRO syndrome. Gene. 2013;516(2):285–90.

    Article  PubMed  Google Scholar 

  86. Kagami M, Nagasaki K, Kosaki R, Horikawa R, Naiki Y, Saitoh S, et al. Temple syndrome: comprehensive molecular and clinical findings in 32 Japanese patients. Genet Med. 2017;19(12):1356–66.

    Article  PubMed  PubMed Central  Google Scholar 

  87. Barakat AJ, et al. Focal sclerosing glomerulonephritis in a child with Laurence-Moon-Biedl syndrome. Child Nephrol Urol. 1990;10(2):109–11.

    CAS  PubMed  PubMed Central  Google Scholar 

  88. Baumstark A, et al. Novel PHF6 mutation p.D333del causes Borjeson-Forssman-Lehmann syndrome. J Med Genet. 2003;40(4):450.

    Article  Google Scholar 

  89. Jenkins D, et al. RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity. Am J Hum Genet. 2007;80(6):1162–70.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  90. Pereira PM, et al. Coffin-Lowry Syndrome. Eur J Hum Genet. 2010;18(6):627–33.

    Article  PubMed  Google Scholar 

  91. El Chehadeh-Djebbar S, et al. Changing facial phenotype in Cohen syndrome: towards clues for an earlier diagnosis. Eur J Hum Genet. 2013;21(7):736–42.

    Article  PubMed  Google Scholar 

  92. Kline AD, et al. Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement. Nat Rev Genet. 2018;19(10):649–66.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  93. Miao ZM, et al. Identification of a novel mutation in a pseudohypoparathyroidism family. Int J Endocrinol. 2011;509549

    Google Scholar 

  94. Ma W, et al. Novel microdeletion in the X chromosome leads to Kallmann syndrome, Icthyosis, Obesity and Strabismus. Front Genet. 2020;11:596.

    Article  PubMed  PubMed Central  Google Scholar 

  95. Berges-Raso I, et al. Kallmann syndrome and ichtyosis: a case of contiguous gene deletion syndrome. Endocrinol Diabetes Metab Case Rep. 2017;170083

    Google Scholar 

  96. Torga AP, et al. Hypogonadotropic hypogonadism and Kleefstra Syndrome due to a pathogenic variant in the EHMT1 gene: an underrecognized association. Case Rep Endocrinol. 2018;4283267

    Google Scholar 

  97. Sharda S, et al. MOMO syndrome with holoprosencephaly and cryptorchidism: expanding the spectrum of the new obesity syndrome. Case Rep Genet. 2011;839650

    Google Scholar 

  98. Butler MG. Prader-Willi syndrome: obesity due to genomic imprinting. Curr Genomics. 2011;12(3):204–15.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  99. Milani D, et al. Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management. Ital J Pediatr. 2015;41(4)

    Google Scholar 

  100. Thaker VV, et al. Whole exome sequencing identifies RAI1 mutation in a morbidly obese child diagnosed with ROHHAD syndrome. J Clin Endocrinol Metab. 2015;100(5):1723–30.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  101. Bertini V, et al. Maternal uniparental disomy 14 (Temple syndrome) as a result of Robertsonian translocation. Mol Syndromol. 2017;8(3):131–8.

    Google Scholar 

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Duis, J., Butler, M.G. (2022). Monogenic and Syndromic Causes of Obesity. In: Butler, M.G., Lee, P.D.K., Whitman, B.Y. (eds) Management of Prader-Willi Syndrome. Springer, Cham. https://doi.org/10.1007/978-3-030-98171-6_4

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