Literature DB >> 3115102

Do some patients with Seckel syndrome have hematological problems and/or chromosome breakage?

M G Butler, B D Hall, R N Maclean, C B Lozzio.   

Abstract

We report on a 12-yr-old female and a 14-yr-old male with Seckel syndrome. The 12-yr-old female had pancytopenia, which is seen occasionally in patients with Seckel syndrome and is also a feature of Fanconi anemia, a well-recognized autosomal recessive dwarfism syndrome with chromosome instability. Chromosome breakage analysis of both of our patients also indicated chromosome instability. We suggest that there may be a subgroup of Seckel syndrome patients with chromosome instability and/or hematological problems.

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Year:  1987        PMID: 3115102      PMCID: PMC5494982          DOI: 10.1002/ajmg.1320270318

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

1.  Familial dwarfism associated with microcephaly, mental retardation and anaemia.

Authors:  C UPJOHN
Journal:  Proc R Soc Med       Date:  1955-05

2.  Seckel's dwarfism: analysis of chromosome breakage and sister chromatid exchanges.

Authors:  J Cervenka; H Tsuchiya; T Ishiki; M Suzuki; H Mori
Journal:  Am J Dis Child       Date:  1979-05

3.  Constitutional hypoplastic anemia associated with familial "bird-headed" dwarfism (Seckel syndrome).

Authors:  J S Lilleyman
Journal:  Am J Pediatr Hematol Oncol       Date:  1984

Review 4.  Studies of microcephalic primordial dwarfism I: approach to a delineation of the Seckel syndrome.

Authors:  F Majewski; T Goecke
Journal:  Am J Med Genet       Date:  1982-05

5.  Seckel syndrome: an overdiagnosed syndrome.

Authors:  E Thompson; M Pembrey
Journal:  J Med Genet       Date:  1985-06       Impact factor: 6.318

6.  Studies of microcephalic primordial dwarfism II: the osteodysplastic type II of primordial dwarfism.

Authors:  F Majewski; M Ranke; A Schinzel
Journal:  Am J Med Genet       Date:  1982-05
  6 in total
  11 in total

1.  Intrauterine programming of ageing.

Authors:  Oscar Fernandez-Capetillo
Journal:  EMBO Rep       Date:  2009-12-11       Impact factor: 8.807

2.  Deletion of the developmentally essential gene ATR in adult mice leads to age-related phenotypes and stem cell loss.

Authors:  Yaroslava Ruzankina; Carolina Pinzon-Guzman; Amma Asare; Tony Ong; Laura Pontano; George Cotsarelis; Valerie P Zediak; Marielena Velez; Avinash Bhandoola; Eric J Brown
Journal:  Cell Stem Cell       Date:  2007-06-07       Impact factor: 24.633

3.  Acute myeloid leukaemia in a patient with Seckel syndrome.

Authors:  A Hayani; C R Suarez; Z Molnar; M LeBeau; J Godwin
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318

4.  A mouse model of ATR-Seckel shows embryonic replicative stress and accelerated aging.

Authors:  Matilde Murga; Samuel Bunting; Maria F Montaña; Rebeca Soria; Francisca Mulero; Marta Cañamero; Youngsoo Lee; Peter J McKinnon; Andre Nussenzweig; Oscar Fernandez-Capetillo
Journal:  Nat Genet       Date:  2009-07-20       Impact factor: 38.330

Review 5.  Primordial dwarfism: overview of clinical and genetic aspects.

Authors:  Preeti Khetarpal; Satrupa Das; Inusha Panigrahi; Anjana Munshi
Journal:  Mol Genet Genomics       Date:  2015-09-01       Impact factor: 3.291

6.  Nek1 kinase associates with ATR-ATRIP and primes ATR for efficient DNA damage signaling.

Authors:  Shizhou Liu; Chu Kwen Ho; Jian Ouyang; Lee Zou
Journal:  Proc Natl Acad Sci U S A       Date:  2013-01-23       Impact factor: 11.205

7.  Chromosomal instability at common fragile sites in Seckel syndrome.

Authors:  Anne M Casper; Sandra G Durkin; Martin F Arlt; Thomas W Glover
Journal:  Am J Hum Genet       Date:  2004-08-12       Impact factor: 11.025

8.  Seckel-like syndrome or Seckel variants?

Authors:  Mathew Punnachalil Cherian
Journal:  Ann Saudi Med       Date:  2004 Nov-Dec       Impact factor: 1.526

9.  New PCNT candidate missense variant in a patient with oral and maxillofacial osteodysplasia: a case report.

Authors:  Ken-Ichi Aoyama; Minoru Kimura; Hiroshi Yamazaki; Masahiro Uchibori; Rena Kojima; Yuko Osawa; Kazuyoshi Hosomichi; Yoshihide Ota; Masayuki Tanaka; Shiro Yamada; Gen Nishimura
Journal:  BMC Med Genet       Date:  2019-07-16       Impact factor: 2.103

10.  Palatoplasty in a patient with Seckel syndrome.

Authors:  Ramneesh Garg; Sanjeev Uppal; Rajinder Mittal; Anju Grewal; Dinesh Sood; Sheerin Shah
Journal:  Ann Maxillofac Surg       Date:  2012-01
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