Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1978-2-18
|
pubmed:abstractText |
Clinical and laboratory data are presented for two patients with a dyshaematopoietic disorder, and monosomy 7 in their bone marrow cells. The first patient, a 55-year-old woman, had been treated with chlorambucil for an ovarian carcinoma. After 4 years an oligoblastic myeloid leukaemia was diagnosed and she later died with an acute transformation of the disease. The second patient, a 21-year-old male, has had a dyserythropoietic anaemia with transient pancytopenia for over 5 years without any signs of malignancy. The possible relationship between therapy, the monosomy 7 and the other bone marrow abnormalities is briefly discussed. From an analysis of the data of these and comparable cases in the literature it appears that loss of chromosome No. 7 material is often associated with erythropoietic disorders such as erythroid hyperplasia and erythraemia. The reduction or absence of the Colton blood group antigens found in our patients and in a few other monosomy 7 cases also points to an abnormality of the red cell line.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0007-1048
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
37
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
101-9
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:588470-Adolescent,
pubmed-meshheading:588470-Bone Marrow,
pubmed-meshheading:588470-Chromosome Aberrations,
pubmed-meshheading:588470-Chromosome Disorders,
pubmed-meshheading:588470-Chromosomes, Human, 6-12 and X,
pubmed-meshheading:588470-Female,
pubmed-meshheading:588470-Humans,
pubmed-meshheading:588470-Karyotyping,
pubmed-meshheading:588470-Male,
pubmed-meshheading:588470-Middle Aged,
pubmed-meshheading:588470-Myeloproliferative Disorders
|
pubmed:year |
1977
|
pubmed:articleTitle |
Monosomy 7 in two patients with a myeloproliferative disorder.
|
pubmed:publicationType |
Journal Article,
Case Reports
|