References
- Bhambhani V, Muenke M. Noonan Syndrome. Am Fam Physician.2014 Jan 1; 89 (1): 37-43
- Mendez HM, Opitz JM. Noonan syndrome: a review. Am J Med Genet. 1985;21(3):493–506.
- Shaw AC, Kalidas K, Crosby AH, Jeffery S, Patton MA. The natural history of Noonan syndrome: a long-term follow-up study. Arch Dis Child. 2007;92(2):128–132.
- Tidyman WE, Rauen KA. The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulation. Curr Opin Genet Dev. 2009;19(3):230–236.
- Allanson JE, Roberts AE. Noonan syndrome. Gene-Tests: Reviews. National Center for Biotechnology Information. http://www.ncbi.nlm.nih.gov/books/NBK1124 Accessed May 23, 2021.
- Allanson JE, Hall JG, Hughes HE, Preus M, Witt RD. Noonan syndrome: the changing phenotype. Am J Med Genet. 1985;21(3):507–514.
- Baldassarre G, Mussa A, Dotta A, Banaudi E, Forzano S, Marinosci A, et al. Prenatal features of Noonan syndrome: prevalence and prognostic value. Prenat Diagn. 2011;31(10):949–954.
- Natraj Setty H.S, Shankar S., Patil R., Santosh J., Yeriswamy M.C., Babu R. et al. Combined cardiac anomalies in Noonan syndrome: A case report. Int J Surg Case Rep. 2020; 72:32-36. Doi: 10.1016/j.ijscr.2020.05.048. Epub 2020 May 30. PMID: 32506025; PMCID: PMC7276397.
- Colquitt JL, Noonan JA. Cardiac findings in Noonan syndrome on long-term follow-up. Congenit. Heart Dis. 2014 Mar-Apr;9(2):144-50. Doi: 10.1111/chd.12102. Epub 2013 Jun 10.
- Vujanovic M, Stankovic-Babic G., Cekic S. Noonan Syndrome – case report. Acta Medica Medianae. 2014; 53(2). UDC: 616007-053.2-071:617.7. Doi:10.5633/amm.2014.0209
- Jaouadi H, Chehida AB, Kraoua L, Etchevers HC, Argiro L, Kasdallah N et al. A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation. Genet Res (Camb). 2019 Apr 29;101: e6. Doi: 10.1017/ S0016672319000041. PMID: 31030682; PMCID: PMC7045029.
- Veselka J, Anavekar NS, Charron P. Hypertrophic obstructive cardiomyopathy. Lancet. 2017 Mar 25;389(10075):12531267. Doi: 10.1016/S0140-6736(16)31321-6. Epub 2016 Nov 30.
- Elliott PM, Anastasakis A, Borger MA, Borggrefe M, Cecchi F, Charron P et al. ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC). Eur Heart J. 2014; 35(39):2733-79. 10.1093/eurheartj/ehu284
- Thompson D, Patrick-Esteve J, Surcouf JW, Rivera D, Castellanos B, Desai P et al. RAF1 variants causing biventricular hypertrophic cardiomyopathy in two preterm infants: further phenotypic delineation and review of literature. Clin Dysmorphol. 2017 Oct;26(4):195-199. Doi: 10.1097/MCD.0000000000000194. PMID: 28777121.
- Levin MD, Saitta SC, Gripp KW, Wenger TL, Ganesh J, Kalish JM et al. Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients. Am J Med Genet A. 2018 Aug; 176(8): 1711–1722. Doi: 10.1002/ ajmg.a.38854. Epub 2018 Jul 28. PMID: 30055033; PMCID: PMC6107379.