Duchenne muscular dystrophy‐rhabdomyosarcoma, ichthyosis vulgaris/acute monoblastic leukemia: Association of rare genetic disorders and childhood malignant diseases
2002; Alan R. Liss, Inc.; Volume: 39; Issue: 1 Linguagem: Inglês
10.1002/mpo.10043
ISSN1096-911X
AutoresZsuzsanna Jakab, István Szegedi, Erzsébet Balogh, Csongor Kiss, Éva Oláh,
Tópico(s)Virus-based gene therapy research
ResumoMedical and Pediatric OncologyVolume 39, Issue 1 p. 66-68 Brief Report Duchenne muscular dystrophy-rhabdomyosarcoma, ichthyosis vulgaris/acute monoblastic leukemia: Association of rare genetic disorders and childhood malignant diseases Zsuzsanna Jakab MD, PhD, Zsuzsanna Jakab MD, PhD Department of Pediatrics, Medical and Health Science Center, University of Debrecen, Debrecen, HungarySearch for more papers by this authorIstván Szegedi MD, István Szegedi MD Department of Pediatrics, Medical and Health Science Center, University of Debrecen, Debrecen, HungarySearch for more papers by this authorErzsébet Balogh PhD, Erzsébet Balogh PhD Department of Pediatrics, Medical and Health Science Center, University of Debrecen, Debrecen, HungarySearch for more papers by this authorCsongor Kiss MD, PhD, Csongor Kiss MD, PhD Department of Pediatrics, Medical and Health Science Center, University of Debrecen, Debrecen, HungarySearch for more papers by this authorÉva Oláh MD, PhD, DSc, Corresponding Author Éva Oláh MD, PhD, DSc [email protected] Department of Pediatrics, Medical and Health Science Center, University of Debrecen, Debrecen, HungaryDepartment of Pediatrics, MHSC, University of Debrecen, H-4012 Debrecen, P.O. Box 32, Hungary.Search for more papers by this author Zsuzsanna Jakab MD, PhD, Zsuzsanna Jakab MD, PhD Department of Pediatrics, Medical and Health Science Center, University of Debrecen, Debrecen, HungarySearch for more papers by this authorIstván Szegedi MD, István Szegedi MD Department of Pediatrics, Medical and Health Science Center, University of Debrecen, Debrecen, HungarySearch for more papers by this authorErzsébet Balogh PhD, Erzsébet Balogh PhD Department of Pediatrics, Medical and Health Science Center, University of Debrecen, Debrecen, HungarySearch for more papers by this authorCsongor Kiss MD, PhD, Csongor Kiss MD, PhD Department of Pediatrics, Medical and Health Science Center, University of Debrecen, Debrecen, HungarySearch for more papers by this authorÉva Oláh MD, PhD, DSc, Corresponding Author Éva Oláh MD, PhD, DSc [email protected] Department of Pediatrics, Medical and Health Science Center, University of Debrecen, Debrecen, HungaryDepartment of Pediatrics, MHSC, University of Debrecen, H-4012 Debrecen, P.O. Box 32, Hungary.Search for more papers by this author First published: 19 May 2002 https://doi.org/10.1002/mpo.10043Citations: 17AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES 1 Méhes K. Mild errors of morphogenesis in malignancy: macroscopic manifestation of genetic instability? Med Pediatr Oncol 2000; 34: 111–112. 2 Quesnel S, Malkin D. Genetic predisposition to cancer and familial cancer syndromes. Pediatr Clin N Am 1997; 44: 791–808. 3 Koscielniak E, Jurgens H, Winkler K, et al. Treatment of soft tissue sarcoma in childhood and adolescence. A report of the German Cooperative Soft Tissue Sarcoma Study. Cancer 1992; 70: 2557–2567. 4 Creutzig U, Ritter J, Zimmermann M, et al. Improved treatment results in high-risk pediatric acute myeloid leukemia patients after intensification with high-dose cytarabine and mitoxanthrone: results of Study Acute Myeloid Leukemia—Berlin–Frankfurt–Munster 93. J Clin Oncol 2001; 19: 2705–2713. 5 Love DR, Davies KE. Duchenne muscular dystrophy. The gene and the protein. Mol Biol Med 1989; 6: 7–17. 6 Pappo AS, Shapiro DN, Crist WM. Rhabdomyosarcoma: biology and treatment. Pediatr Clin N Am 1997; 44: 953–972. 7 Goldsmith LA. The ichthyoses. Prog Med Genet 1976; 1: 185–210. 8 Scheimberg I, Harper JI, Malone M, et al. Inherited ichthyoses: a review of the histology of the skin. Pediatr Pathol Lab Med 1996; 16: 359–378. 9 Sybert VP, Dale BA, Holbrook KA. Ichthyosis vulgaris: identification of a defect in synthesis of filagrin correlated with an absence of keratohyaline granules. J Invest Dermatol 1985; 84: 191–194. 10 Spelman LJ, Strutton GM, Robertson IM, Weedon D. Aquired ichthyosis in bone marrow transplant recipients. J Am Acad Dermatol 1996; 35: 17–20. 11 Shimamoto Y, Narisawa Y, Suga K, et al. Relationship between autoantibody and dermatosis in myelodysplastic syndrome. Haematologia 1993; 25: 253–261. 12 Al-Sheyyab M, El-Shanti H, Todd D, Shurman A. Autosomal recessive lamellar ichthyosis and acute lymphoid leukemia. Eur J Hum Genet 1996; 4: 105–107. 13 Mallory SB, Kletzel M, Turley CP. X-linked ichthyosis with acute lymphoblastic leukemia. Arch Dermatol 1988; 124: 22–24. 14 Drachtman RA, Alter BP. Dyskeratosis congenita. Dermatol Clin 1995; 13: 33–39. 15 Schmitt TA, Degos L. Leucemies familiales. Bull Cancer 1978; 65: 83–88. 16 Keith L, Bouri ER, Ames B, et al. Leukemia in twins: antenatal and postnatal factors. Acta Genet Med Genellol (Roma) 1976; 25: 336–341. 17 Bittles AH, Mason WM, Greene J, et al. Reproductive behaviour and health in consanguineous marriages. Science 1991; 252: 789–794. Citing Literature Volume39, Issue1July 2002Pages 66-68 ReferencesRelatedInformation
Referência(s)