Mosaic Down's syndrome with de novo 45,XX,-21,-22,+t(21q;22q)/46,XX,-21,+t(21q;21q) rearrangement.
نویسندگان
چکیده
The occurrence of mosaic Down's syndrome with two independent Robertsonian translocation cell lines is very rare. Such a patient is reported here, in whom an unbalanced Robertsonian translocation between two chromosomes 21 was detected in the majority of cells. The patient also revealed a minor cell line with a second Robertsonian translocation involving a chromosome 21 and a 22. The chromosome translocations detected in this patient were de novo in origin.
منابع مشابه
An unusual case of mosaic Down's syndrome involving two different Robertsonian translocations.
A baby girl with some of the stigmata of Down's syndrome was found to be a mosaic with three different cell lines: 45,XX,-13,-21,+t(13q21q)/(46,XX/46,XX, -21,+t(21q21q). The chromosome rearrangements detected in this patient appear to have arisen de novo. In the normal cell line the terminal end of the p arm of one chromosome 21 is thought to have been damaged. It seems probable that this is re...
متن کاملRisk Assessment and Prenatal Diagnosis in a Recent Pregnancy in a Family with a Child with Down Syndrome due to t (21q;21q)
We here present a family with a boy with 21q;21qtype translocation of Down syndrome. He was six years old. His clinical presentation included the classical findings of Down syndrome. We found 46,XY, -21, + t(21q;21q) chromosomal consitution in all metaphases obtained from peripheral blood cells of the child (Figure 1). Then we examined his parents. Both spouses were 32 years old. They were heal...
متن کاملA rare non-Robertsonian translocation involving chromosomes 15 and 21.
CONTEXT Robertsonian translocations (RT) are among the most common balanced structural rearrangements in humans and comprise complete chromatin fusion of the long arm of two acrocentric chromosomes. Nevertheless, non-Robertsonian translocation involving these chromosomes is a rare event. CASE REPORT We report a de novo unbalanced translocation involving chromosomes 15 and 21. The newborn was ...
متن کاملAre de novo rea(21;21) chromosomes really de novo?
We report a rare case of recurrent trisomy 21 caused by an isochromosome 21q and what is very likely to be maternal germ-line cell mosaicism. Over 90% of cases of rob(21;21) reported in the literature are due to an isochromosome 21q, with a risk of recurrence of more than 10%.
متن کاملTransient leukemoid proliferation of the cytogenetically unbalanced +21 cell line of a constitutional mosaic boy.
A newborn without any signs of Down's syndrome was found to have an acute proliferation that remitted without drug therapy. Chromosomal analysis of blood, bone marrow, and skin cells revealed that the child was a constitutional mosaic with normal cells and a low number of cells in which one no. 21 chromosome was replaced by a probably isochromosome for the no. 21 long arm: 46,XY/46,XY,i(21q). T...
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ورودعنوان ژورنال:
- Journal of medical genetics
دوره 21 5 شماره
صفحات -
تاریخ انتشار 1984