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PMID: 8556820 Published · ppublish English Case Reports Journal Article Review

Clinical phenotype associated with terminal 2q37 deletion.

Clinical genetics ·Vol. 48 ·No. 3 ·1995-09-00 ·Pages 134-9

Conrad B, Dewald G, Christensen E, Lopez M, Higgins J, Pierpont ME

Abstract

Three children with deletions of the terminal portion of the long arm of chromosome 2 [del (2) (q37)] are described and their clinical findings compared to published cases of 2q terminal deletions. Common clinical findings include development delay, macrocephaly, frontal bossing, depressed nasal bridge and cardiac anomaly. Hypotonia and repetitive behavior are also seen during different times of development. The facial characteristics of children with 2q terminal deletions are not uniform, but development delay is a constant finding. Chromosomal analysis of such children using high resolution banding may uncover the diagnosis of a small chromosomal deletion.

MeSH Terms
Abnormalities, Multiple/genetics Chromosome Deletion Chromosomes, Human, Pair 2 Humans Infant Karyotyping Male Phenotype
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Conrad B
Department of Maternal-Fetal Medicine, United Hospital, St. Paul, Minnesota, USA.
Dewald G
Christensen E
Lopez M
Higgins J
Pierpont M E
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1995-09-00
Pages
134-9
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
Corrections
CommentIn
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