Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2002-7-31
pubmed:abstractText
Partial monosomy of distal 10q is an uncommon chromosomal disorder. Its characteristic features include growth retardation, psychomotor delay, facial dysmorphia, congenital heart disease, and anogenital/urinary tract anomalies. Reported here is a female infant at age 4 months who was diagnosed with a de novo deletion of the long arm of chromosome 10, with a breakpoint at 10q26. Using the Bayley scales of infant development II, she was found to have mild psychomotor delay. We also review the related literature of partial deletion of the long arm of chromosome 10.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:issn
1608-8115
pubmed:author
pubmed:issnType
Print
pubmed:volume
43
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
153-6
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed:articleTitle
Monosomy of chromosome 10q26 with mild psychomotor retardation: report of one case.
pubmed:affiliation
Department of Pediatrics, China Medical College Hospital, Taichung, Taiwan.
pubmed:publicationType
Journal Article, Case Reports