DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY

Yıl 2011, Cilt: 8 Sayı: 4, 338 - 341, 01.12.2011

Resit Koken Aysegül Bukulmez Gulengul Koken Betul Eser Hale Samlı Tevhide Demır Mustafa Solak

https://izlik.org/JA99DN97SP

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DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY

https://izlik.org/JA99DN97SP

Öz

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Anahtar Kelimeler

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Kaynakça

• Jones KL. XYY Syndrome. Smith’s Recognizable Patterns of Human Malformation 5 th ed. Philadelphia: WB Saunders 1997:70-71.
• Ford CE, Jones KW, Miller OJ, et al. The chromosomes in a patient showing both mongolism and the Klinefelter syndrome. Lancet 1959;1:709-10.
• Kovaleva NV, Mutton DE. Epidemiology of double aneu- ploidies involving chromosome 21 and the sex chromo- somes. Am J Med Genet A 2005;134:24-32.
• Li QY, Tsukishiro S, Nakagawa C, et al. Parental origin and cell stage of non-disjunction of double trisomy in spon- taneous abortion. Congenit Anom (Kyoto) 2005;45:21-5.
• Al-Aish MS, Dodson WE, Plato CC. Down's syndrome with XYY: 48,XYY, G+. Am J Dis Child 1971;121:444-6.
• McLean SD. Congenital Anomalies. In: Mhairi G. MacDonald MDM, Mary M.K. Seshia, ed. Avery’s Neonatology Pathophysiology& Management of the Newborn. 6 th ed. Philadelphia: Lippincott Williams& Wilkins, 2005:893- 913.
• Parmar RC, Muranjan MN, Swami S. Trisomy 21 with XYY. Indian J Pediatr 2002;69:979-81.
• Widness JA, Pueschel SM, Pezzullo JC, Clemons GK. Elevated erythropoietin levels in cord blood of newborns with Down's syndrome. Biol Neonate 1994;66:50-5.
• Gollop TR, Naccache NF, Auler-Bittencourt E, et al. Prenatal diagnosis of 48,XYY, +21 ascertained through ul- trasound anomalies. Am J Med Genet 1991;39:76-7.