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PMID: 641949 Published · ppublish English Case Reports Journal Article

Partial trisomy for short and long arm of chromosome no. 5: Two cases of two possible syndromes.

Journal of medical genetics ·Vol. 15 ·No. 2 ·1978-04-00 ·Pages 143-7

Zabel B, Baumann W, Gehler J, Conrad G

Abstract

We report 2 patients from different families with malformation-retardation syndromes caused by a partial trisomy of the long and of the short arm of chromosome 5, respectively (case 1: 46,XX,der(3),t(3;5)(p27;p13)mat; case 2: 46,XY,der(22),t(5;22)(q33;q13)pat). Several members of these families were balanced translocation carriers. Our cases are compared with those cited in the literature. The possibility of delineating a 5p- and a 5q-partial-trisomy syndrome is discussed.

MeSH Terms
Abnormalities, Multiple/genetics Azure Stains Chromosomes/ultrastructure Chromosomes, Human, 4-5 Female Growth Disorders/genetics Humans Infant Karyotyping Male Motor Activity Phenotype Trisomy
Chemicals
Azure Stains
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Zabel B
Baumann W
Gehler J
Conrad G
References (11)
11 references, click to expand
  1. [FAMILIAL SEGREGATION OF A 5-13 TRANSLOCATION DETERMINING PARTIAL MONOSOMY AND A TRISOMY OF THE SHORT ARM OF THE 5 CHROMOSOME: "CAT CRY" DISEASE AND ITS "RECEPROCAL"].
    C R Hebd Seances Acad Sci. 1964 Jun 8;258:5767-70 PMID: 14161436
  2. Banding in human chromosomes treated with trypsin.
    Nat New Biol. 1972 Jan 12;235(54):52-4 PMID: 4109406
  3. Assignment by deletion of human red cell acid phosphatase gene locus to the short arm of chromosome 2.
    Nat New Biol. 1973 Jun 27;243(130):271-4 PMID: 4515493
  4. A partial trisomy 5p syndrome.
    Birth Defects Orig Artic Ser. 1975;11(5):191-200 PMID: 1218213
  5. Karyotype with chromosomal abnormality with various inherited defects in the offspring (recombination aneusomy).
    Humangenetik. 1973 Dec 20;20(4):355-9 PMID: 4768111
  6. [Segregation of a balanced translocation t(5p-;Gp+)].
    Ann Genet. 1968 Dec;11(4):247-52 PMID: 5306368
  7. [Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"].
    Ann Genet. 1966 Sep;9(3):113-22 PMID: 5298289
  8. Partial trisomy 5 with a carrier parent t(5p-;9p+).
    Clin Genet. 1976 Apr;9(4):437-40 PMID: 1261081
  9. Partial trisomy for the long arms of chromosome no. 5 due to insertion and further 'aneusomie de recombinaison'.
    J Med Genet. 1975 Dec;12(4):418-23 PMID: 1219125
  10. Familial translocation, t(2;5) (p23; g31).
    Clin Genet. 1975 Aug;8(2):112-6 PMID: 1175316
  11. Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families.
    Am J Hum Genet. 1967 Jul;19(4):586-603 PMID: 6036276
Article Info
Journal
Journal of medical genetics
Abbr.
J Med Genet
ISSN
0022-2593
Published
1978-04-00
Pages
143-7
Language
English
Region
England
NLM ID
2985087R
PMCID
PMC1013664
Subset
IM
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