Diagnóstico prenatal de inversión pericentrica del cromosoma cinco de novo en una paciente con gestación a término sin complicaciones posteriores

Chang HP, Chion JY, Chen JY, Su PH. Prenatal cytogenetic diagnosis in Taiwan: a nationwide population-based study. The Journal of Maternal-Fetal & Neonatal Medicine [Internet]. 2016 [citado 01 Feb 2017];0(0):1–8. Disponible en: http://doi.org/10.1080/14767058.2016.1255191.

Petersson K, Lindkvist M, Persson M, Conner P, Åhman A, Mogren I. Prenatal diagnosis in Sweden 2011 to 2013—a register-based study. BMC Pregnancy and Childbirth [Internet].

[citado 01 Feb 2017];16(1):1-13. Disponible en: http://doi.org/10.1186/s12884-016-1165-8.

Cheng JF. Chromosome 5. Encyclopedia of life sciences [Internet]. 2006 [citado 17 Feb 2017];0(0):1-8. Disponible en: http://onlinelibrary.wiley.com/doi/10.1038/npg.els.0005814/

abstract.

Mandal A. ¿Cuál es el Cromosoma 5 ? NEWS Med [Internet]. 2014 [citado 10 Feb 2017];0(0):1–5. Disponible en: http://www.news-medical.net/health/What-is-Chromosome-5-(Spanish).aspx.

Schmutz J, Martin J, Terry A, Couronne O, Grimwood J, Lowry S, et al. The DNA sequence and comparative analysis of human chromosome 5. Nature [Internet].2004 [citado 08 Feb 2017];431(1):268–274. Disponible en: http://www.ncbi.nlm.nih.gov/pubmed/15372022

Kaffenberger B. Inversion. Understanding cromosomas disorders [Internet]. 2014 [citado 08 Feb 2017];0(0):1-12. Disponible en: http://www.rarechromo.org/information/Other/Inversions%20FTNW.pdf

Bernicot I, Dechanet C, MacE A, Hedon B, Hamamah S, Pellestor F, et al. Predictive value of sperm-FISH analysis on the outcome of preimplantation genetic diagnosis (PGD) for a pericentric inversion inv5(p15.3q11.2) carrier. Hum Reprod [Internet]. 2010 [citado 10 Feb 2017];25(7):1818–1823. Disponible en: http://www.fertstert.org/article/S0015-

(09)03005-2/abstract

Conditions G. Genetics home reference. Genet Home Ref [Internet]. 2017[citado 05 Feb 2017];0(0):1–7. Disponible en: https://ghr.nlm.nih.gov/chromosome/5.pdf.

Siddiqi R, Gilbert F. Chromosome 5. Genetic Test [Internet]. 2004 (citado 11 Feb 2017).7(2): 169- 87. Disponible en: http://online.liebertpub.com/doi/abs/10.1089/109065703322146902

Evans J a. Diaphragmatic defects and limb deficiencies - taking sides. Am J Med Genet A [Internet]. 2007 (citado 09 Feb 2017);143(18):2106–2112. Disponible en: https://www.ncbi.nlm.nih.gov/pubmed/17701998

Saultz JN, Kaffenberger BH, Taylor M, Heerema NA, Klisovic R. Novel Chromosome 5 Inversion Associated With PDGFRB Rearrangement in Hypereosinophilic Syndrome. JAMA Dermatology [Internet]. 2016 (citado 12 Feb 2017);152(12):1391-1392. Disponible en: http://archderm.jamanetwork.com/article.aspx?doi=10.1001/jamadermatol.2016.3175

Ferguson JS, Bosworth J, Min T, Mercieca J, Holden CA. Eosinophilic fasciitis associated with hypereosinophilia, abnormal bone-marrow karyotype and inversion of chromosome 5. Clin Exp Dermatol [Internet]. 2014 (citado 11 Feb 2017);39(2):150–153. Disponible en: https://www.ncbi.nlm.nih.gov/pubmed/24237445

Jones ML, Murden SL, Brooks C, Maloney V, Manning RA, Gilmour KC, et al. Disruption of AP3B1 by a chromosome 5 inversion:1 new disease mechanism in Hermansky-Pudlak syndrome type 2. BMC Med Genet [Internet]. 2013 (citado 11 Feb 2017);0(0):1-14. Disponible en: http://link.springer.com/article/10.1186/1471-2350-14-42

De Oliveira FM, Scrideli CA, Queiroz RG, Tone LG. Acute lymphoblastic leukemia with inv(5)(q13q31) in a pediatric patient. Cancer Genet Cytogenet [Internet]. 2006 (citado 11

Feb 2017);165(1):81–82. Disponible en: http://www.ncbi.nlm.nih.gov/pubmed/16490602.

Butcher BW, Wilson KS, Kroft SH, Collins RH. Acute leukemia with B-lymphoid and myeloid differentiation associated with an inv ( 5 )( q13q33 ) in an adult patient. Cancer Genet Cytogenet. 2005 (citado 11 Feb 2017);157(1):62–66. Disponible en: https://www.ncbi.nlm.nih.gov/pubmed/15676149

Concolino D, Iembo MA, Rossi E, Giglio S, Coppola G, Miraglie E, et al. Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsions. J Med Genet

[Internet]. 2002 (citada 11 Feb 2017);39(3):214–216. Disponible en: http://www.ncbi.nlm.nih.gov/entrez/query. fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_

uids=11897828.

Dutta MK, Gundgurthi A, Garg MK, Pakhetra R. Cryptorchidism due to chromosome 5q inversion duplication. J Assoc Physicians India [Internet]. 2013 (citada 11 Feb 2017);61(1):925–927. Disponible en: https://www.ncbi.nlm.nih.gov/pubmed/24968555

Ohnuki Y, Torii C, Kosaki R, Yagihashi T, Sago H, Hayashi K, et al. Cri-du-chat syndrome cytogenetically cryptic recombination aneusomy of chromosome 5: Implications in recurrence

risk estimation. Mol Syndromol [Internet]. 2010 (citada 12 Feb 2017);1(2):95–98. Disponible en: https://www.ncbi.nlm.nih.gov/pubmed/21045963

Schmidt T, Bartels I, Liehr T, Burfeind P, Zoll B, Shoukier M. A family with an inverted tandem duplication 5q22.1q23.2. Cytogenet Genome Res [Internet]. 2012 (citado 11 Feb 2017); 139(1):65–70. Disponible en: https://www.karger.com/Article/Abstract/342914

Pierce BA. Genética un enfoque conceptual [Internet]. 5 ed. Estados Unidos: Panamericana; 2014. [Citado 11 Feb 2017]. Disponible en: https://books.google.es/books?id=ALR9bgLtFhYC&

printsec=frontcover&hl=es&source=gbs_ge_summary_r&cad=0#v=onepage&q&f=false

Bernal Luz Mery, López Greizy. Diagnóstico prénatal: retrospectiva. Nova. 2014; 12( 21 ): 23-36.

Almonacid Urrego Carmen Cecilia, Camarillo Romero María del Socorro, Gil Murcia Zulay, Medina Medina Claudia Yasmin,Rebellón Marulanda Jennifer Viviana, Mendieta Zerón Hugo. Evaluación de factores de riesgo asociados a enfermedad cardiovascular en jóvenes universitarios de la Localidad Santafé en Bogotá, Colombia. Nova. 2016; 14(25): 9-17.

González Devia Johanna L., Monroy Romero Paola A., Almonacid Urrego Carmen C.. Homocisteína y otros factores de riesgo cardiovascular en niños de educación básica primaria

del Colegio Distrital Manuel Elkin Patarroyo, Bogotá, D.C.Colombia. Estudio piloto. Nova. 2017 ; 15( 27 ): 103-117.