Abstract
A mentally retarded boy was found to have an unusual chromosomal mosaicism [46,XY, del(18) (q22)/46,XY,iso psu dic(18)(q23)]. The clinical manifestations are compatible with the 18q- syndrome. The chromosome alteration was defined by high resolution banding and fluorescence in situ hybridization (FISH). A mechanism to explain the origin of the two cell lines is presented and discussed.
MeSH terms
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Abnormalities, Multiple / genetics
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Child, Preschool
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Chromosome Aberrations / genetics*
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Chromosome Banding
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Chromosome Deletion
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Chromosome Disorders
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Chromosomes, Human, Pair 18*
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Dwarfism / genetics
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Humans
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In Situ Hybridization, Fluorescence
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Intellectual Disability / genetics*
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Karyotyping
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Male
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Mosaicism*
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Respiratory Tract Infections / genetics
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Sister Chromatid Exchange