Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features.
case_report · Level V
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- Record sourced from PubMed, PMID 8487285.
- Also identified by PMC identifier 1016348.
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Abstract
We report on a retarded infant with minor dysmorphic features in whom deletion 16 and duplication 19q were discovered. The karyotype is 46,XX,del(16) (q13.08-21.05),dup(19)(q13.13-13.2). The origin and significance of the aberrant chromosomes are unknown.
Medical subject headings
- Abnormalities, Multiple
- Chromosome Aberrations
- Chromosome Deletion
- Chromosomes, Human, Pair 16
- Chromosomes, Human, Pair 19
- Intellectual Disability