Literature DB >> 20327419

Autosomal Trisomies and Partial Trisomy Syndromes: (With Presentation of Two Cases of Partial Trisomy for the E Group of Chromosomes).

W A Zaleski.   

Abstract

The establishing of 46 chromosomes as the normal complement in man and the report of the sex chromatin bodies in buccal smears were followed by reports of trisomies and other abnormal patterns of the X and Y chromosomes in Klinefelter's and Turner's syndromes. Abnormal autosomal complements were described in mongolism, in the E-trisomy syndrome, the D-trisomy syndrome, in the Sturge-Weber syndrome, Waldenstrom's macroglobulinemia, benign congenital hypotonia, atrial septal defect and in the schizoid personality. Certain of these conditions, as well as the "oral-facial-digital" syndrome, were also found to exist as partial trisomies. The mechanism of a trisomy is one of non-disjunction and of partial trisomy translocation or insertion. Two cases of the partial trisomy in the E group are described; these are of especial interest because of the familial incidence, longer survival and male sex occurrence, features which are rarely seen in the full E-trisomy syndrome.

Entities:  

Year:  1963        PMID: 20327419      PMCID: PMC1921116     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN: 0008-4409            Impact factor:   8.262


  23 in total

1.  A presumptive human XXY/XX mosaic.

Authors:  C E FORD; P E POLANI; J H BRIGGS; P M BISHOP
Journal:  Nature       Date:  1959-04-11       Impact factor: 49.962

2.  Multiple congenital anomaly associated with an extra autosome.

Authors:  M D CRAWFURD
Journal:  Lancet       Date:  1961-07-01       Impact factor: 79.321

3.  A probable XXYY sex determining mechanism in a mentally defective male with Klinefelter's syndrome.

Authors:  D H CARR; M L BARR; E R PLUNKETT
Journal:  Can Med Assoc J       Date:  1961-04-22       Impact factor: 8.262

4.  Chromosomal trisomy associated with the Sturge-Weber syndrome.

Authors:  M D HAYWARD; B D BOWER
Journal:  Lancet       Date:  1960-10-15       Impact factor: 79.321

5.  Hypertrophied frenuli, oligophrenia, famflial trembling and anomalies of the hand. Report of four casesin one family and a forme fruste in another.

Authors:  R J GORLIN; V E ANDERSON; C R SCOTT
Journal:  N Engl J Med       Date:  1961-03-09       Impact factor: 91.245

6.  Chromosomal aberrations in man.

Authors:  S RAPPOPORT; W D KAPLAN
Journal:  J Pediatr       Date:  1961-09       Impact factor: 4.406

7.  Chromosome identification and the Denver report.

Authors:  K PATAU
Journal:  Lancet       Date:  1961-04-29       Impact factor: 79.321

8.  Partial-trisomy syndromes. I. Sturge-Weber's disease.

Authors:  K PATAU; E THERMAN; D W SMITH; S L INHORN; B F PICKEN
Journal:  Am J Hum Genet       Date:  1961-09       Impact factor: 11.025

9.  Klinefelter's syndrome in a ten-month-old mongolian idiot: report of a case with chromosome analysis.

Authors:  J T LANMAN; B S SKLARIN; H L COOPER; K HIRSCHHORN
Journal:  N Engl J Med       Date:  1960-11-03       Impact factor: 91.245

10.  A case of human intersexuality having a possible XXY sex-determining mechanism.

Authors:  P A JACOBS; J A STRONG
Journal:  Nature       Date:  1959-01-31       Impact factor: 49.962

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  1 in total

1.  [Diagnosis of arthrogryposis multiplex congenita].

Authors:  E Hertel; S Stotz; H M Jacobi; J D Murken
Journal:  Arch Orthop Unfallchir       Date:  1969
  1 in total

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