Literature DB >> 1121016

Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome.

N C Magnelli, E Therman.   

Abstract

A severely mentally retarded man displayed the following main symptoms: short stature, microcephaly, antimongoloid slant of palpebral fissures, big ears with hyperplastic helices, imperfect dental enamel, short and webbed neck, short arms, short hands, brachymetaphalangy, short second fingers, broad thumbs, short metatarsal bones, and unusually big first toes. It seems almost certain that the syndrome was caused by a chromosome deletion involving about half of 12p which was present in all of the lymphocytes examined.

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Year:  1975        PMID: 1121016      PMCID: PMC1013240          DOI: 10.1136/jmg.12.1.105

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  5 in total

1.  LONGITUDINAL DIFFERENTIATION OF CHROMOSOMES AND THE POSSIBILITY OF INTERSTITIAL TELOMERES.

Authors:  T C HSU
Journal:  Exp Cell Res       Date:  1963       Impact factor: 3.905

2.  FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.

Authors:  I A UCHIDA; K N MCRAE; M RAY
Journal:  Am J Hum Genet       Date:  1965-09       Impact factor: 11.025

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

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

4.  Cytogenetics in mentally defective children with anomalies: a controlled study.

Authors:  R L Summitt
Journal:  J Pediatr       Date:  1969-01       Impact factor: 4.406

5.  Cytological studies on a human ring chromosome.

Authors:  P Cooke; R R Gordon
Journal:  Ann Hum Genet       Date:  1965-11       Impact factor: 1.670

  5 in total
  8 in total

1.  Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent.

Authors:  C J Van Der Burgt; G F Merkx; A H Janssen; J C Mulder; R F Suijkerbuijk; D F Smeets
Journal:  J Med Genet       Date:  1992-10       Impact factor: 6.318

2.  A cytogenetic survey of 200 unclassifiable mentally retarded children with congenital anomalies and 200 normal controls.

Authors:  A T Tharapel; R L Summitt
Journal:  Hum Genet       Date:  1977-07-26       Impact factor: 4.132

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.  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

5.  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

6.  Chromosome 12p Deletion Spanning the GRIN2B Gene Presenting With a Neurodevelopmental Phenotype: A Case Report and Review of Literature.

Authors:  Navin Mishra; Elizabeth Kouzmitcheva; Angela Orsino; Berge A Minassian
Journal:  Child Neurol Open       Date:  2016-04-04

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

Review 8.  Variable Phenotypes of Epilepsy, Intellectual Disability, and Schizophrenia Caused by 12p13.33-p13.32 Terminal Microdeletion in a Korean Family: A Case Report and Literature Review.

Authors:  Ji Yoon Han; Joonhong Park
Journal:  Genes (Basel)       Date:  2021-06-29       Impact factor: 4.096

  8 in total

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