Hepatic Tumor as Antenatal Presentation of Costello Syndrome
Abstract
Keywords
Full Text:
PDFReferences
Gripp KW, Rauen KA. Costello syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, et al, editors. GeneReviews® [monograph on the Internet]. Seattle (WA): University of Washington; 1993–2020 [cited 2019 Aug 29]. Available from: https://www.ncbi.nlm.nih.gov/books/ NBK1507/
Kratz CP, Rapisuwon S, Reed H, Hasle H, Rosenberg PS. Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes. Am J Med Genet C Semin Med Genet 2011;157C:83-9.
Lin AE, O'Brien B, Demmer LA, Almeda KK, Blanco CL, Glasow PF, et al. Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardia. Prenat Diagn 2009; 29:682-90.
Quelin C, Loget P, Rozel C, D'Herve D, Fradin M, Demurger F, et al. Fetal costello syndrome with neuromuscular spindles excess and p.Gly12Val HRAS mutation. Eur J Med Genet 2017;60:395-8.
Bend EG, Louie RJ, Stevenson RE. Fetal edema, not overgrowth, is associated with neonatal lethal Costello syndrome due to the HRAS p.Gly12Val mutation. Clin Dysmorphol 2019; 28:71-3.
Kuniba H, Pooh RK, Sasaki K, Shimokawa O, Harada N, Kondoh T, et al. Prenatal diagnosis of Costello syndrome using 3D ultrasonography amniocentesis confirmation of the rare HRAS mutation G12D. Am J Med Genet A 2009;149A:785-7
Myers A, Bernstein JA, Brennan ML, Curry C, Esplin ED, Fisher J, et al. Perinatal features of the RASopathies: Noonan syndrome, cardiofaciocutaneous syndrome and Costello syndrome. Am J Med Genet A 2014;164A:2814-21.
Uemura R, Tachibana D, Kurihara Y, Pooh RK, Aoki Y, Koyama M. Prenatal findings of hypertrophic cardiomyopathy in a severe case of Costello syndrome. Ultrasound Obstet Gynecol 2016;48:799-800.
Burkitt-Wright EM, Bradley L, Shorto J, McConnell VP, Gannon C, Firth HV, et al. Neonatal lethal Costello syndrome and unusual dinucleotide deletion/insertion mutations in HRAS predicting p.Gly12Val. Am J Med Genet A 2012;158A:1102- 10.
van der Burgt I, Kupsky W, Stassou S, Nadroo A, Barroso C, Diem A, et al. Myopathy caused by HRAS germline mutations: implications for disturbed myogenic differentiation in the presence of constitutive HRas activation. J Med Genet 2007; 44:459-62.
Hague J, Hackett G, Acerini C, Park SM. Prenatal genetic diagnosis of Costello syndrome in a male fetus with recurrent HRAS mutation p.Gly12Ser. Prenat Diagn 2017;37:409-11.
Fernandez-Medarde A, Santos E. Ras in cancer and developmental diseases. Genes Cancer 2011;2:344-58.
Bertola D, Buscarilli M, Stabley DL, Baker L, Doyle D, Bartholomew DW, et al. Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp. Am J Med Genet A 2017;173:1309-18.
Refbacks
- There are currently no refbacks.
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.