Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1998-7-27
pubmed:abstractText
A 12-year-old girl developed ataxia that gradually progressed. At age 18 the patient presented with mental retardation, cachectic dwarfism, microcephalus, and a progeroid appearance but no photosensitive skin lesions or deafness. On analysis of fibroblasts, unscheduled DNA synthesis was reduced to 50% of normal, but colony-forming ability after ultraviolet irradiation was normal. The symptoms and phenotype of the patient were distinguished from those in Cockayne syndrome and xeroderma pigmentosum. This case is interesting because the defect in DNA repair after ultraviolet irradiation was detected in a patient with neurologic disturbances but without photosensitive skin lesions.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0887-8994
pubmed:author
pubmed:issnType
Print
pubmed:volume
18
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
358-61
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:9588536-Abnormalities, Multiple, pubmed-meshheading:9588536-Adolescent, pubmed-meshheading:9588536-Cachexia, pubmed-meshheading:9588536-Cells, Cultured, pubmed-meshheading:9588536-Cerebellar Ataxia, pubmed-meshheading:9588536-Cerebellum, pubmed-meshheading:9588536-DNA, pubmed-meshheading:9588536-DNA Repair, pubmed-meshheading:9588536-Diagnosis, Differential, pubmed-meshheading:9588536-Dwarfism, pubmed-meshheading:9588536-Female, pubmed-meshheading:9588536-Fibroblasts, pubmed-meshheading:9588536-Humans, pubmed-meshheading:9588536-Intellectual Disability, pubmed-meshheading:9588536-Magnetic Resonance Imaging, pubmed-meshheading:9588536-Microcephaly, pubmed-meshheading:9588536-Phenotype, pubmed-meshheading:9588536-Progeria, pubmed-meshheading:9588536-Ultraviolet Rays, pubmed-meshheading:9588536-Xeroderma Pigmentosum
pubmed:year
1998
pubmed:articleTitle
A DNA repair defect in a patient with ataxia, mental retardation, and short stature.
pubmed:affiliation
Department of Pediatrics, Jichi Medical School, Tochigi, Japan.
pubmed:publicationType
Journal Article, Comparative Study, Case Reports