Literature DB >> 1176124

Short arm deletion of chromosome 12: report of two new cases.

E Orye, M Craen.   

Abstract

Two boys (W.M. and C.P.) are described, in each of whom a short-arm deleted C chromosome was apparently present. The clinical findings on W.M. are stenosis of the sagittal sutura associated with atrophy of the nervus opticus and mental retardation, and on C.P. osteogenesis imperfecta. An analysis of the G- and Q-banding patterns revealed in each patient a 12p-- chromosome. The deletion involved most of band p12 as shown by length measurements on G-banded chromosomes. Both cases were compared to proven and presumed cases of 12p-- from literature, but no common clinical phenotype could be demonstrated.

Entities:  

Mesh:

Year:  1975        PMID: 1176124     DOI: 10.1007/bf00284808

Source DB:  PubMed          Journal:  Humangenetik        ISSN: 0018-7348


  6 in total

1.  Autosomal deletions 46,XY,del(12)(p11) and 46,XY-46,XY,del(5)(p13) with no effect on physical or mental development.

Authors:  U Friedrich; J Nielsen
Journal:  Humangenetik       Date:  1974-02-21

2.  Banding pattern analysis of human chromosomes by use of a urea treatment technique.

Authors:  Y Shiraishi; T H Yosida
Journal:  Chromosoma       Date:  1972       Impact factor: 4.316

3.  Identification of human chromosomes by DNA-binding fluorescent agents.

Authors:  T Caspersson; L Zech; C Johansson; E J Modest
Journal:  Chromosoma       Date:  1970       Impact factor: 4.316

4.  Localization of the human lactate dehydrogenase B gene on the short arm of chromosome 12.

Authors:  K Mayeda; L Weiss; R Lindahl; M Dully
Journal:  Am J Hum Genet       Date:  1974-01       Impact factor: 11.025

5.  Clinical, cytogenetic and autoradiographic studies in 10 cases with rare chromosome disorders II. Cases 3,4 and 5.

Authors:  M K Moore; E Engel
Journal:  Ann Genet       Date:  1970-06

6.  [Partial monosomy of a C group chromosome (Cp-)].

Authors:  C Laurent; A Nivelon; E Hartman; G Guerrier
Journal:  Ann Genet       Date:  1968-12
  6 in total
  7 in total

1.  12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech.

Authors:  Julien Thevenon; Patrick Callier; Joris Andrieux; Bruno Delobel; Albert David; Sylvie Sukno; Delphine Minot; Laure Mosca Anne; Nathalie Marle; Damien Sanlaville; Marlène Bonnet; Alice Masurel-Paulet; Fabienne Levy; Lorraine Gaunt; Sandra Farrell; Cédric Le Caignec; Annick Toutain; Virginie Carmignac; Francine Mugneret; Jill Clayton-Smith; Christel Thauvin-Robinet; Laurence Faivre
Journal:  Eur J Hum Genet       Date:  2012-06-20       Impact factor: 4.246

2.  Lethal osteogenesis imperfecta associated with 46,XY,inv(7)(p13q22) karyotype.

Authors:  A S Knisely; A Richardson; D Abuelo; S Casey; D B Singer
Journal:  J Med Genet       Date:  1988-05       Impact factor: 6.318

3.  Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features.

Authors:  Allen N Lamb; Jill A Rosenfeld; Nicholas J Neill; Michael E Talkowski; Ian Blumenthal; Santhosh Girirajan; Debra Keelean-Fuller; Zheng Fan; Jill Pouncey; Cathy Stevens; Loren Mackay-Loder; Deborah Terespolsky; Patricia I Bader; Kenneth Rosenbaum; Stephanie E Vallee; John B Moeschler; Roger Ladda; Susan Sell; Judith Martin; Shawnia Ryan; Marilyn C Jones; Rocio Moran; Amy Shealy; Suneeta Madan-Khetarpal; Juliann McConnell; Urvashi Surti; Andrée Delahaye; Bénédicte Heron-Longe; Eva Pipiras; Brigitte Benzacken; Sandrine Passemard; Alain Verloes; Bertrand Isidor; Cedric Le Caignec; Gwen M Glew; Kent E Opheim; Maria Descartes; Evan E Eichler; Cynthia C Morton; James F Gusella; Roger A Schultz; Blake C Ballif; Lisa G Shaffer
Journal:  Hum Mutat       Date:  2012-04       Impact factor: 4.878

4.  10p- syndrome associated with multiple chromosomal abnormalities.

Authors:  F Prieto; L Badia; J A Moreno; P Barbero; F Asensi
Journal:  Hum Genet       Date:  1978-12-18       Impact factor: 4.132

5.  Interstitial 12p deletion involving more than 40 genes in a patient with postnatal microcephaly, psychomotor delay, optic nerve atrophy, and facial dysmorphism.

Authors:  Anne Hoppe; Jan Heinemeyer; Eva Klopocki; Luitgard M Graul-Neumann; Birgit Spors; Petra Bittigau; Angela M Kaindl
Journal:  Meta Gene       Date:  2014-01-11

6.  12p deletion spectrum syndrome: a new case report reinforces the evidence regarding the potential relationship to autism spectrum disorder and related developmental impairments.

Authors:  Marcio Leyser; Bruno Leonardo Dias; Ana Luiza Coelho; Marcio Vasconcelos; Osvaldo J M Nascimento
Journal:  Mol Cytogenet       Date:  2016-10-04       Impact factor: 2.009

7.  A 3.06-Mb interstitial deletion on 12p11.22-12.1 caused brachydactyly type E combined with pectus carinatum.

Authors:  Jia Huang; Hong-Yan Liu; Rong-Rong Wang; Hai Xiao; Dong Wu; Tao Li; Ying-Hai Jiang; Xue Zhang
Journal:  Chin Med J (Engl)       Date:  2019-07-20       Impact factor: 2.628

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.