Trisomy for the short arm of chromosome No. 10
Penchaszadeh, V.B.; Coco, R.
Journal de Genetique Humaine 25(3): 221-227
1977
ISSN/ISBN: 0021-7743 PMID: 591928 Document Number: 114084
To the authors knowledge there is a single previous report of confirmed trisomy for the short arm of chromosome No 10 (Hustinx et al., 1974). In this paper we present a further case of trisomy 10p, resulting from 3 : 1 segregation of maternal balanced translocation, t(3;10)(q;11), in a female infant aged 7 months and showing numerous somatic anomalies.
Document emailed within 1 workday
Related Documents
Zerova-Liubimova, T.E.; Rigel, M.; Smul'skaia, N.A.; Evseenkova, E.G.; Gorovenko, N.G.; Shintzel, A. 2004: Molecular-cytogenetic identification of partial trisomy of a short arm of chromosome 8 Tsitologiia i Genetika 38(4): 55-61Rethoré, M.O.; Larget-Piet, L.; Abonyi, D.; Boeswillwald, M.; Berger, R.; Carpentier, S.; Cruveiller, J.; Dutrillau, B.; Lafourcade, J.; Penneau, M.; Lejeune, J. 1970: 4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity Annales de Genetique 13(4): 217-232
Simon, N.; Hunyadi, J.; Szörényi, A.; Szemere, G. 1973: Deletion of the short arm of chromosome 18 and trisomy 18 in a pair of siblings with unusual form of porphyria Der Hautarzt; Zeitschrift für Dermatologie Venerologie und verwandte Gebiete 24(5): 185-189
Verma, R.S.; Dosik, H.; Wexler, I.B. 1977: Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q Journal de Genetique Humaine 25(4): 295-301
Yeatman, G.W.; Riccardi, V.M. 1976: Partial trisomy of chromosome 14: (+14q-) Birth Defects Original Article Series 12(5): 119-124
Rogóyski, A.; Babel, M.; Tronowska, T.D. 1983: Partial trisomy of chromosome 22 in an infant Pediatria Polska 58(6): 561-564
Mino, M.; Kasubuchi, Y.; Goto, M.; Onouchi, Z.; Kusunoki, T. 1976: Chromosome 8 trisomy mosaic syndrome Jinrui Idengaku Zasshi. Japanese Journal of Human Genetics 21(2): 69-78
Plaja, A.; Mediano, C.; Farran, I.; Vendrell, T.; Toran, N.; Gili, T.; Sanchez, M.A.; Sarret, E. 1998: Trisomy (12p) with telocentric and pseudoisodicentric chromosome formation in a fetus Annales de Genetique 41(1): 52-55
Crandall, B.F.; Muller, H.M.; Bass, H.N. 1973: Partial trisomy of chromosome number 15 identified by trypsin-Giemsa banding American Journal of Mental Deficiency 77(5): 571-578
Grozdea, J.; Colombies, P.; Verdier, J. 1973: Quantitative multienzymatic deficiency and chromosome malsegregation: patients with trisomy 21 and their parents La Nouvelle Presse Medicale 2(19): 1289-1291
El-Bassyouni, H.T.; El-Gerzawy, A.M.S.; Mohamed, A.M.; Kamel, A.K.; Hussein, H.A.; Thomas, M.M.; El-Ruby, M. 2014: Terminal 2q deletion and partial trisomy chromosome 15q: a clinical and cytogenetic study Genetic Counseling 25(2): 151-158
Rossetti, A.; Taliani, U.; Del Sante, G.; Manini, M.; Castello, S. 1982: Chronic myeloid leukemia, Ph negative with chromosome 8 trisomy. A case report Acta Bio-Medica de l'Ateneo Parmense 53(4): 243-247
Luciani, J.M.; Devictor, M.; Boué, J.; Morazzani, M.R.; Boué, A.; Stahl, A. 1978: Oocyte meiosis in a trisomy 18 fetus. Behavior of the supernumerary chromosome and identification of the 18 bivalent Annales de Genetique 21(4): 215-218
Obersztyn, E.; Stankiewicz, P.; Bocian, E.; Stańczak, H.; Mazurczak, T. 1996: Partial trisomy of chromosome 13--diagnosis confirmed with the FISH in situ hybridization technique Pediatria Polska 71(3): 247-252
Fineman, R.M.; Kidd, K.K.; Johnson, A.M.; Breg, W.R. 1976: Increased frequency of heterozygotes for alpha1 antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21 Nature 260(5549): 320-321
Erdem, H.B.; Sahin, I.; Tasdemir, S.; Tatar, A. 2016: Partial Trisomy 5p12-Q 11.2 Resulting from a Marker Chromosome: A new Case Report with Attention Deficit Hyperactivity Disorder Genetic Counseling 27(3): 295-303
Turkina, A.G.; Domracheva, E.V.; Vorontsova, A.V.; Aseeva, E.A.; Vinogradova, O.I.; Stakhina, O.V.; Gusarova, G.A.; Diagileva, O.A.; Semenova, E.A.; Vakhrusheva, M.V.; Kolosheĭnova, T.I.; Abakumov, E.M.; Chelysheva, E.I.; Goriacheva, S.R.; Ivanova, T.V.; Zakharova, E.S.; Kolosova, L.I.; Zakharova, A.V.; Naumova, I.N.; Diachenko, L.V.; Kulikov, S.M.; Kovaleva, L.G.; Khoroshko, N.D. 2009: Trisomy of chromosome 8 in Ph-negative cells of the bone marrow in patients with chronic myeloid leukemia treated with inhibitors of BCR-ABL tyrosine kinases Terapevticheskii Arkhiv 81(7): 29-36
D'Oelsnitz, M.; Ayraud, N.; de Swarte, M.; Vaillant, J.M.; Darcourt, G. 1970: A case of deletion of short arm of chromosome 18 Pediatrie 25(2): 213-214
Serville, F.; Allain, D.; Broustet, A.; Martin, C.; Gachet, M.; Babin, J.P.; Cenraud, J. 1976: Partial deletion of the short arm of the chromosome 9 Annales de Genetique 19(2): 143
Fryns, J.P. 1996: Gingival fibromatosis and partial duplication of the short arm of chromosome 2 (dup(2)(p13-->p21)) Annales de Genetique 39(1): 54-55