We report on 2 unrelated cases of duplication of distal 3p due to balanced maternal translocation t(3;6)(p23;q27) and t(2;3)(p25;p23) respectively. One family was ascertained through the unbalanced offspring and the other through echographic examination of the balanced carrier mother. These cases confirm that dup(3)(p2----pter) results in a characteristic syndrome with distinctive facial appearance. In family 2 inspection of a photograph of a deceased sib was sufficient to conclude that he was affected. The patient in family 2 had cyclopia. Since holoprosencephaly was also reported by Martin and Steinberg [1983], we conclude that this anomaly appears to be a sign of the syndrome. The duplication usually derives from a maternal balanced translocation, in most cases from adjacent-1 segregation. However, family 2 was ascertained through a balanced female carrier who inherited the translocation from the father. We have noted that the second chromosome (which varies without apparent preferences) involved in these translocations is broken consistently at a distal band.

Dup(3)(p2----pter) in two families, including one infant with cyclopia.

ZUFFARDI, ORSETTA
1985-01-01

Abstract

We report on 2 unrelated cases of duplication of distal 3p due to balanced maternal translocation t(3;6)(p23;q27) and t(2;3)(p25;p23) respectively. One family was ascertained through the unbalanced offspring and the other through echographic examination of the balanced carrier mother. These cases confirm that dup(3)(p2----pter) results in a characteristic syndrome with distinctive facial appearance. In family 2 inspection of a photograph of a deceased sib was sufficient to conclude that he was affected. The patient in family 2 had cyclopia. Since holoprosencephaly was also reported by Martin and Steinberg [1983], we conclude that this anomaly appears to be a sign of the syndrome. The duplication usually derives from a maternal balanced translocation, in most cases from adjacent-1 segregation. However, family 2 was ascertained through a balanced female carrier who inherited the translocation from the father. We have noted that the second chromosome (which varies without apparent preferences) involved in these translocations is broken consistently at a distal band.
1985
20
341
348
7
Abnormalities; Multiple; genetics, Adult, Amniotic Fluid; cytology, Chromosome Aberrations, Chromosome Banding, Chromosomes; Human; 1-3, Chromosomes; 6-12 and X, Eye Abnormalities, Female, Humans, Infant; Newborn, Karyotyping, Lymphocytes; ultrastructure, Male, Pedigree, Pregnancy, Prenatal Diagnosis, Syndrome, Translocation; Genetic
http://dx.doi.org/10.1002/ajmg.1320200217
8
info:eu-repo/semantics/article
262
G., Gimelli; C., Cuoco; M., Lituania; M., Cordone; M., Aricò; E., Bianchi; P., Maraschio; Zuffardi, Orsetta
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/454526
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