Literature DB >> 3812587

Autosomal recessive nonsyndromal microcephaly with normal intelligence.

A S Teebi, S A Al-Awadi, A G White.   

Abstract

Autosomal recessive microcephaly is usually associated with moderate to severe mental retardation. An apparently new autosomal recessive disorder comprising a characteristic facial appearance associated with microcephaly and normal intelligence, immunodeficiency, and increased risk for lymphoreticular malignancies has been described recently. We report on a large Arab kindred with frequent consanguineous marriages and eight cases in five sibships with microcephaly, peculiar facies, and normal intelligence. Of these cases, two died of an acute lymphoreticular malignancy or bronchopneumonia. Immunological and chromosomal studies carried out for the three affected living sibs were normal. The existence of an autosomal recessive nonsyndromal variant of microcephaly with normal intelligence is proposed and discussed.

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Year:  1987        PMID: 3812587     DOI: 10.1002/ajmg.1320260214

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


  10 in total

1.  Microcephaly-cardiomyopathy: a new autosomal recessive phenotype?

Authors:  I M Winship; D L Viljoen; P M Leary; M M De Moor
Journal:  J Med Genet       Date:  1991-09       Impact factor: 6.318

2.  Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: genetic relationship to ataxia telangiectasia.

Authors:  N G Jaspers; R D Taalman; C Baan
Journal:  Am J Hum Genet       Date:  1988-01       Impact factor: 11.025

3.  Microcephaly and childhood non-Hodgkin's lymphoma.

Authors:  A Dluzniewska; D Tredowska-Skoczen; J Armata; J Tacik
Journal:  Arch Dis Child       Date:  1995-11       Impact factor: 3.791

Review 4.  Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings.

Authors:  C Geoffrey Woods; Jacquelyn Bond; Wolfgang Enard
Journal:  Am J Hum Genet       Date:  2005-03-31       Impact factor: 11.025

5.  A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34.

Authors:  L Moynihan; A P Jackson; E Roberts; G Karbani; I Lewis; P Corry; G Turner; R F Mueller; N J Lench; C G Woods
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

6.  Severe microcephaly with normal intellectual development: the Nijmegen breakage syndrome.

Authors:  A J Green; J R Yates; A M Taylor; P Biggs; G M McGuire; C M McConville; C J Billing; N D Barnes
Journal:  Arch Dis Child       Date:  1995-11       Impact factor: 3.791

Review 7.  Autosomal recessive disorders among Arabs: an overview from Kuwait.

Authors:  A S Teebi
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

8.  ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome.

Authors:  C J Curry; P O'Lague; J Tsai; H T Hutchison; N G Jaspers; D Wara; R A Gatti; H T Hutchinson
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

Review 9.  Autosomal Recessive Primary Microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum.

Authors:  Saqib Mahmood; Wasim Ahmad; Muhammad J Hassan
Journal:  Orphanet J Rare Dis       Date:  2011-06-13       Impact factor: 4.123

10.  A novel single base pair duplication in WDR62 causes primary microcephaly.

Authors:  Verena Rupp; Sobiah Rauf; Ishrat Naveed; Christian Windpassinger; Asif Mir
Journal:  BMC Med Genet       Date:  2014-10-11       Impact factor: 2.103

  10 in total

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