Literature DB >> 912941

Phenotypic correlations in patients with ring chromosome 22.

A G Hunter, M Ray, H S Wang, D R Thompson.   

Abstract

This paper reports two patients with a ring 22 chromosome which has been confirmed by Q-banding. The literature contains 19 patients with a ring G-group chromosome which has been shown by chromosome banding to be a ring 22. The most commonly reported features in affected patients have included: retardation with disproportionate verbal delay, reduced head circumference, hypotonia, unsteady gait, large ears with abnormal configuration, and epicanthic folds. The importance of these, as well as other, less often noted findings, is discussed in relation to a possible r(22) syndrome.

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Year:  1977        PMID: 912941     DOI: 10.1111/j.1399-0004.1977.tb00933.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  11 in total

1.  A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome.

Authors:  J L Watt; I A Olson; A W Johnston; H S Ross; D A Couzin; G S Stephen
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

2.  Segregation of a 22 ring chromosome in three generations.

Authors:  C Stoll; M P Roth
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

3.  Monosomy 22 with mosaicism.

Authors:  M S Moghe; Z M Patel; J J Peter; L M Ambani
Journal:  J Med Genet       Date:  1981-02       Impact factor: 6.318

4.  Partial trisomy 6p with karyotype 46,XY,der(22), t(6;22)(p22;q13)mat.

Authors:  G B Côté; S Papadakou-Lagoyanni; S Sbyrakis
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

5.  22q13.3 deletion syndrome: clinical and molecular analysis using array CGH.

Authors:  S U Dhar; D del Gaudio; J R German; S U Peters; Z Ou; P I Bader; J S Berg; M Blazo; C W Brown; B H Graham; T A Grebe; S Lalani; M Irons; S Sparagana; M Williams; J A Phillips; A L Beaudet; P Stankiewicz; A Patel; S W Cheung; T Sahoo
Journal:  Am J Med Genet A       Date:  2010-03       Impact factor: 2.802

Review 6.  Human chromosome 22.

Authors:  J C Kaplan; A Aurias; C Julier; M Prieur; M F Szajnert
Journal:  J Med Genet       Date:  1987-02       Impact factor: 6.318

7.  Molecular studies of DiGeorge syndrome.

Authors:  W J Fibison; M Budarf; H McDermid; F Greenberg; B S Emanuel
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

8.  Ring chromosome 22 in a mentally retarded child and mosaic 45,XX,-15,-22,+t(15;22)(p11;q11)/46,XX,r(22)/46,XX karyotype in the mother.

Authors:  J P Fryns; H Van den Berghe
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

9.  Metachromatic leucodystrophy (MLD) in a patient with a constitutional ring chromosome 22.

Authors:  M B Coulter-Mackie; J Rip; M D Ludman; J Beis; D E Cole
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

10.  An r(22)(p11 leads to q13) in a moderately mentally retarded girl.

Authors:  V Aller; J A Abrisqueta; M L de Torres; M A Martín-Lucas; A Pérez-Castillo; J Del Mazo
Journal:  Hum Genet       Date:  1979-10-01       Impact factor: 4.132

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