Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1984-4-18
pubmed:abstractText
Sixteen cases of terminal deletions and 17 cases of interstitial deletions of the long arm of chromosome 7 have been reported to date. We present two new cases of the former and three of the latter. The somatic changes in these patients are tabulated and an update on the anomalies associated with the various cytogenetic entities is presented. Changes found in over one-third of patients with 7q terminal deletion syndrome include: developmental delay, pre- and postnatal growth retardation, generalized hypotonia, abnormal electroencephalograms with or without seizures, feeding problems in infancy, microcephaly, prominent forehead, ocular hypertelorism, eye defects, broad nasal bridge, bulbous nasal tip, auricular malformations, micrognathia, chest abnormalities, genital malformations in males, and abnormal palmar and plantar creases. Evidence for the localization of the Kidd blood group gene on chromosome 7 distal to band q32, as suggested by previous reports, is reviewed; we conclude that the evidence does not warrant placement of the gene in this region of the genome.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0148-7299
pubmed:author
pubmed:issnType
Print
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
437-50
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:6199974-Abnormalities, Multiple, pubmed-meshheading:6199974-Child, pubmed-meshheading:6199974-Chromosome Banding, pubmed-meshheading:6199974-Chromosome Deletion, pubmed-meshheading:6199974-Chromosome Mapping, pubmed-meshheading:6199974-Chromosomes, Human, 6-12 and X, pubmed-meshheading:6199974-Craniofacial Dysostosis, pubmed-meshheading:6199974-Dermatoglyphics, pubmed-meshheading:6199974-Developmental Disabilities, pubmed-meshheading:6199974-Electroencephalography, pubmed-meshheading:6199974-Female, pubmed-meshheading:6199974-Humans, pubmed-meshheading:6199974-Infant, pubmed-meshheading:6199974-Intellectual Disability, pubmed-meshheading:6199974-Karyotyping, pubmed-meshheading:6199974-Kidd Blood-Group System, pubmed-meshheading:6199974-Male, pubmed-meshheading:6199974-Muscle Hypotonia
pubmed:year
1984
pubmed:articleTitle
Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new cases.
pubmed:publicationType
Journal Article, Case Reports