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Vol. 55. Núm. 5.
Páginas 458-462 (noviembre 2001)
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Vol. 55. Núm. 5.
Páginas 458-462 (noviembre 2001)
Acceso a texto completo
Duplicación invertida del brazo corto del cromosoma 8
Inverted duplication of the short arm of chromosome 8
Visitas
22816
L. Rodríguez Martíneza,
Autor para correspondencia
luisama@eucmos.sim.ucm.es

Correspondencia: ECEMC. Facultad de Medicina. Universidad Complutense. Madrid.Avda. Complutense, s/n. 28040 Madrid
, N. Jiménez Muñoz-Delgadob, C. Nietoc, A. Martínez Carrascald, F. López Grondonaa, M.aL. Martínez Fríasa,e
a Estudio Colaborativo Español de Malformaciones Congénitas (ECEMC). Facultad de Medicina, Universidad Complutense. Madrid.
b Servicios de Obstetricia y Ginecología. Hospital General de Segovia
c Servicios de Pediatría. Hospital General de Segovia
d Servicio de Pediatría. Hospital General de Requena. Valencia
e Departamento de Farmacología. Facultad de Medicina Universidad Complutense. Madrid
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Información del artículo

Se presentan 2 casos con agenesia de cuerpo calloso en los que el estudio citogenético con bandas G de alta resolución reveló una duplicación invertida del brazo corto del cromosoma 8.

La aplicación de técnicas de hibridación in situ (FISH) confirmó la alteración cromosómica en ambos casos, siendo el cariotipo definitivo: 46,XY o XX inv dup del (8) (qter-p23.1::p23.1-p11.2).ish (WCP 8+)(tel 8p-)

Palabras clave:
Duplicación invertida
Agenesia de cuerpo calloso
Cromosoma 8
FISH

We report two cases of agenesis of corpus callosum in which high resolution G-band cytogenetic study revealed inverted duplication of the short arm of chromosome 8.

The application of hybridization techniques with fluorescence in situ hybridization (FISH) confirmed chromosomal alteration in both cases. The definitive karyotype was 46, XY or XX inv dup del (8) (qter-p23.1::p23.1-p11.2).ish(WCP 81) (tel 8p-)

Key words:
Inverted duplication
Agenesis of corpus callosum
Chromosome 8
FISH
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Bibliografía
[1.]
R.G. Weleber, R.S. Verma, W.J. Kimberling, H.G. Fieger, H.A. Lubs.
Duplication-deficient of the short arm of chromosome 8 following artificial insemination.
Ann Genet, 19 (1976), pp. 241-247
[2.]
K.M. Taylor, U. Franke, M.G. Brown, D.L. Goerger, M. Kaufhold.
Inverted tandem (“mirror”) duplications in human chromosomes: inv dup 8p, 4p, 22q.
Am J Med Genet, 1 (1977), pp. 2-19
[3.]
K. Hongell, S. Knuutilla, Y. Westermarck.
Two cases of an abnormal short arm of chromosome 8 (8p+) associated with mental retardation.
Clin Genet, 13 (1978), pp. 237-240
[4.]
J.F. Mattei, M.G. Mattei, J.P. Ardissone, J. Coignet, F. Giraud.
Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8p.
Hum Genet, 53 (1980), pp. 315-321
[5.]
P.K.A. Jensen, C. Junein, S. Despoisse, A. Berseb, T. Thelle, U. Freidrich, et al.
Inverted tandem duplication of the short arm of chromosome 8: a non-random de novo structural aberration in man: localization of the gene for glutathione reductase in sub-band 8p21.1.
Ann Genet, 25 (1982), pp. 207-211
[6.]
J.P. Fryns, A. Kleczkowska, A.M. Dereymaker, M. Hoefnagels, G. Heremans, J. Mrien, et al.
Partial 8p trisomy due to interstitial duplication: karyotype: 46, XX, inv dup(8)(p21.1–p22).
Clin Genet, 28 (1985), pp. 546-549
[7.]
F.J. Dill, M. Schertzer, J. Sandercock, B. Tischler, S. Wood.
Inverted tandem duplication generates a duplication deficiency of chromosome 8p.
Clin Genet, 32 (1987), pp. 109-113
[8.]
A. Kleczkowska, J.P. Fryns, F. D’Hondt, J. Jaeken, H. Van Den Berghe.
Partial duplication 8p due to interstitial duplication: inv dup (8)(p21.1–22): further delineation of the phenotype from birth to adulthood.
Ann Genet, 30 (1987), pp. 47-51
[9.]
N.C. Nevin, P.J. Morrison, J. Jones, M. Mac Reid.
Inverted tandem duplication of 8p12–p23.1 in a child with increase activity of glutathione reductase.
J Med Genet, 27 (1990), pp. 135-136
[10.]
M. Gorinati, D. Caufin, A. Minelli, L. Memo, G. Gaspardo, A. Dodero.
Inv dup (8)(p21.2–22): further case report and a new hypothesis on the origin of the chromosome abnormality.
Clin Genet, 39 (1991), pp. 55-59
[11.]
K.G. Henderson, F.J. Dill, S. Wood.
Characterization of an inversion duplication of the short arm of chromosome 8 by fluorescent insitu hybridization.
Am J Med Genet, 44 (1992), pp. 615-619
[12.]
G.L. Feldman, L. Weiss, M.C. Phlen, R.J. Schroer, D.L. Van Dyke.
Inverted duplication of 8p: ten new patients and review of the literature.
Am J Med Genet, 47 (1993), pp. 482-486
[13.]
A. Minelli, G. Floridia, E. Rossi, M. Clementi, R. Tenconi, L. Camurri, et al.
D8S7 in consistently deleted in inverter duplications of the short arm of chromosome 8 (inv dup 8p).
Hum Genet, 92 (1993), pp. 391-396
[14.]
J.J. Mitchell, M. Vekemans, S. Luscombe, M. Hayden, B. Weber, A. Richter, et al.
U-type excange in a paracentric inversion as possible mechanism of origin of an inverted tandem duplication of chromosome 8.
Am J Med Genet, 49 (1994), pp. 384-387
[15.]
W.J. Guo, F. Callif-Daley, M.C. Zapata, M.E. Miller.
Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
Am J Med Genet, 58 (1995), pp. 230-236
[16.]
C.E. Die-Smulders, J.J. Engelen, C.T. Schrander-Stumpel, L.C. Govaerts, B. De Vries, J.S. Vles.
Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
Am J Med Genet, 59 (1995), pp. 369-374
[17.]
G. Floridia, M. Piantanida, A. Minelli, C. Dellavecchia, E. Rossi, G. Gimelli, et al.
The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications.
Am J Hum Genet, 58 (1996), pp. 785-796
[18.]
A. Yenamandra.
Inverted duplication/deletion of chromosome 8p: mild clinical phenotype.
Am J Med Genet, 82 (1999), pp. 91-93
[19.]
M.D. Macmillin, V. Suri, C. Lytle, C.M. Krauss.
Prenatal diagnosis of inverted duplicated 8p.
Am J Med Genet, 93 (2000), pp. 94-98
[20.]
M.C. Digilio, A. Giannotti, G. Floridia, F. Uccellatore, R. Mingarelli, C. Danesino, et al.
Trisomy-8 syndrome owing to isodicentric 8p chromosomes: Regional assignment of a presumptive gene involved in corpus callosum development.
J Med Genet, 31 (1994), pp. 238-241
[21.]
B.L. Wu, G.H. Schneider, D.E. Sabatino, L.Z. Bozovic, B. Cao, B.R. Korf.
Distal 8p deletion (8)(p23.1): An easily missed chromosome abnormality that may be associated with congenital heart defect and mental retardation.
[22.]
C.T. Kuo, E.E. Morrisey, R. Anandappa, K. Sigrist, M.M. Lu, M.S. Parmacek, et al.
GATA4 transcription factor is required for ventral morphogenesis and heart tube formation.
Genes Dev, 11 (1997), pp. 1048-1060
[23.]
P. Marynen, K. Devriendt, R. Van Dael, J.R. Vermeesch, G. Matthijs, K. Brondum-Nielsen, et al.
The GATA4 gene is located in the critical deletion region for congenital heart defects on chromosome 8p23.1.
Am J Hum Genet, 63 (1998), pp. 7
[24.]
S. Giglio, K.W. Broman, N. Matsumoto, V. Calvari, G. Gimelli, T. Neumann, et al.
Olfactory receptorgene clusters, genomicinversion polymorphisms, and common chromosome rearrangements.
Am J Hum Genet, 68 (2001), pp. 874-883
Copyright © 2001. Asociación Española de Pediatría
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