Literature DB >> 7239510

Incomplete trisomy 22. III. Mosaic-trisomy 22 and the problem of full trisomy 22.

A Schinzel.   

Abstract

A severely growth-retarded female newborn is described, who dies a few hours after birth. About half of the clones and metaphases from an amniotic fluid cell culture (set up at 35th week of gestation) and only 1/27 of the metaphases from a blood lymphocyte culture contained an additional No. 22 chromosome. Abnormal findings in the patient included a complex congenital heart defect, membranous anal atresia without fistula, distal limb hypoplasia, partial cutaneous syndactyly between second and third toes, and a left preauricular pit. On the basis of this case and other reports from the literature arguments for and against the existence of full human trisomy 22 are discussed. The conclusion seems likely, that full trisomy 22 usually presents a lethal condition in man, though at present an occasional survival cannot be excluded.

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Year:  1981        PMID: 7239510     DOI: 10.1007/bf00274677

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  29 in total

1.  [Identification by Q and G bands of chromosome anomalies in spontaneous abortion].

Authors:  J Boué; M J Daketsé; C Deluchat; N Ravisé; F Yvert; A Boué
Journal:  Ann Genet       Date:  1976-12

2.  Balanced homologous translocation t(22q22q) in a phenotypically normal woman with repeated spontaneous abortions.

Authors:  L M Farah; H R de Nazareth; M Dolnikoff; D Delascio
Journal:  Humangenetik       Date:  1975-08-25

3.  A new contribution to the study of 22 trisomy.

Authors:  A Pérez-Castillo; J A Abrisqueta; M A Martin-Lucas; C Goday; J Del Mazo; V Aller
Journal:  Humangenetik       Date:  1975-09-20

4.  A 22/22 translocation carrier with recurrent abortions demonstrated by a Giemsa banding technique,.

Authors:  T Maeda; M Ohno; N Shimada; M Nishida; T Jobo
Journal:  Hum Genet       Date:  1976-02-29       Impact factor: 4.132

5.  Precise identification of various chromosomal abnormalities.

Authors:  K Hirschhorn; M Lucas; I Wallace
Journal:  Ann Hum Genet       Date:  1973-04       Impact factor: 1.670

6.  Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy.

Authors:  H J Kim; L Y Hsu; L C Goldsmith; L Strauss; K Hirschhorn
Journal:  J Med Genet       Date:  1977-04       Impact factor: 6.318

7.  A familial X-22 translocation with an extra X chromosome.

Authors:  M B Jenkins; E Davis; T H Thelen; L Boyd
Journal:  Am J Hum Genet       Date:  1974-11       Impact factor: 11.025

8.  Incomplete trisomy 22. II. Familial trisomy of the distal segment of chromosome 22q in two brothers from a mother with a translocation, t(6;22)(q27;q13).

Authors:  A Schinzel
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Trisomy 22 with 'cat eye' anomaly.

Authors:  J Cervenka; C A Hansen; R A Franciosi; R J Gorlin
Journal:  J Med Genet       Date:  1977-08       Impact factor: 6.318

10.  The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture.

Authors:  A Schinzel; W Schmid; M Fraccaro; L Tiepolo; O Zuffardi; J M Opitz; J Lindsten; P Zetterqvist; H Enell; C Baccichetti; R Tenconi; R A Pagon
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

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  5 in total

1.  Incomplete trisomy 22. II. Familial trisomy of the distal segment of chromosome 22q in two brothers from a mother with a translocation, t(6;22)(q27;q13).

Authors:  A Schinzel
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

2.  Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families.

Authors:  A Schinzel; W Schmid; P Auf der Maur; H Moser; K H Degenhardt; M Geisler; A Grubisic
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

3.  Trisomy 22 in a newborn with multiple malformations.

Authors:  I Voiculescu; E Back; A M Duncan; H Schwaibold; W Schempp
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

4.  Live-born trisomy 22: patient report and review.

Authors:  T Heinrich; I Nanda; M Rehn; U Zollner; E Frieauff; J Wirbelauer; T Grimm; M Schmid
Journal:  Mol Syndromol       Date:  2013-01-11

5.  The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture.

Authors:  A Schinzel; W Schmid; M Fraccaro; L Tiepolo; O Zuffardi; J M Opitz; J Lindsten; P Zetterqvist; H Enell; C Baccichetti; R Tenconi; R A Pagon
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

  5 in total

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