Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn--karyotype: 46,XX,del(2)(q21;q24). 1977

J P Fryns, and B Van Bosstraeten, and H Malbrain, and H Van den Berghe

This report describes a polymalformed female newborn presenting an interstitial deletion of the long arms of chromosome 2. Karyotype: 46,XX,del(2)(q21 q24).

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D007621 Karyotyping Mapping of the KARYOTYPE of a cell. Karyotype Analysis Methods,Analysis Method, Karyotype,Analysis Methods, Karyotype,Karyotype Analysis Method,Karyotypings,Method, Karyotype Analysis,Methods, Karyotype Analysis
D008213 Lymphocyte Activation Morphologic alteration of small B LYMPHOCYTES or T LYMPHOCYTES in culture into large blast-like cells able to synthesize DNA and RNA and to divide mitotically. It is induced by INTERLEUKINS; MITOGENS such as PHYTOHEMAGGLUTININS, and by specific ANTIGENS. It may also occur in vivo as in GRAFT REJECTION. Blast Transformation,Blastogenesis,Lymphoblast Transformation,Lymphocyte Stimulation,Lymphocyte Transformation,Transformation, Blast,Transformation, Lymphoblast,Transformation, Lymphocyte,Activation, Lymphocyte,Stimulation, Lymphocyte
D008214 Lymphocytes White blood cells formed in the body's lymphoid tissue. The nucleus is round or ovoid with coarse, irregularly clumped chromatin while the cytoplasm is typically pale blue with azurophilic (if any) granules. Most lymphocytes can be classified as either T or B (with subpopulations of each), or NATURAL KILLER CELLS. Lymphoid Cells,Cell, Lymphoid,Cells, Lymphoid,Lymphocyte,Lymphoid Cell
D002872 Chromosome Deletion Actual loss of portion of a chromosome. Monosomy, Partial,Partial Monosomy,Deletion, Chromosome,Deletions, Chromosome,Monosomies, Partial,Partial Monosomies
D002900 Chromosomes, Human, 1-3 The large, metacentric human chromosomes, called group A in the human chromosome classification. This group consists of chromosome pairs 1, 2, and 3. Chromosomes A,Group A Chromosomes,Chromosome, Group A,Chromosomes, Group A,Group A Chromosome
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000015 Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. Multiple Abnormalities

Related Publications

J P Fryns, and B Van Bosstraeten, and H Malbrain, and H Van den Berghe
November 1986, American journal of medical genetics,
J P Fryns, and B Van Bosstraeten, and H Malbrain, and H Van den Berghe
February 1991, Anales espanoles de pediatria,
J P Fryns, and B Van Bosstraeten, and H Malbrain, and H Van den Berghe
December 1981, Jinrui idengaku zasshi. The Japanese journal of human genetics,
J P Fryns, and B Van Bosstraeten, and H Malbrain, and H Van den Berghe
December 1982, Journal of medical genetics,
J P Fryns, and B Van Bosstraeten, and H Malbrain, and H Van den Berghe
July 1983, Acta paediatrica Scandinavica,
J P Fryns, and B Van Bosstraeten, and H Malbrain, and H Van den Berghe
December 1993, Clinical genetics,
J P Fryns, and B Van Bosstraeten, and H Malbrain, and H Van den Berghe
March 1984, Jinrui idengaku zasshi. The Japanese journal of human genetics,
J P Fryns, and B Van Bosstraeten, and H Malbrain, and H Van den Berghe
April 1984, Clinical genetics,
J P Fryns, and B Van Bosstraeten, and H Malbrain, and H Van den Berghe
January 1996, American journal of medical genetics,
J P Fryns, and B Van Bosstraeten, and H Malbrain, and H Van den Berghe
February 1988, Clinical genetics,
Copied contents to your clipboard!