Deletion of chromosome 2 (p11-p13): case report and review.
case_report · Level V
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- Record sourced from PubMed, PMID 8411037.
- Also identified by PMC identifier 1016464.
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Abstract
The case of a young man with del(2) (p11.2p13) is reported. Accounts of previous cases of deletion of the short arm of chromosome 2 are reviewed. Common features include mental retardation, proportional short stature and weight, dysmorphic facial features (a prominent nose, abnormal ears), and abnormal hands. Growth and developmental delay are present during the postnatal period.
Medical subject headings
- Abnormalities, Multiple
- Chromosome Deletion
- Chromosomes, Human, Pair 2
- Intellectual Disability