Literature DB >> 1735087

Familial microcephaly with normal intelligence in a patient with acute lymphoblastic leukemia.

D Heney1, R Mueller, G Turner, G Karbani, J Cadranel, I J Lewis, C C Bailey.   

Abstract

The authors describe a family with two children with microcephaly and normal intelligence, in which acute lymphoblastic leukemia developed in one of the siblings. An autosomal recessive pattern of inheritance is suggested by the pedigree. This is consistent with the literature, which the authors reviewed. All of the patients have similar phenotypic features, with some demonstrating chromosomal instability. It is important to recognize this syndrome because of the increased risk of lymphoreticular malignancy.

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Year:  1992        PMID: 1735087     DOI: 10.1002/1097-0142(19920215)69:4<962::aid-cncr2820690421>3.0.co;2-w

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  5 in total

1.  Autozygosity mapping, complex consanguinity, and autosomal recessive disorders.

Authors:  R F Mueller; D T Bishop
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

2.  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

3.  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 4.  Dissecting the Genetic and Etiological Causes of Primary Microcephaly.

Authors:  Francesca Jean; Amanda Stuart; Maja Tarailo-Graovac
Journal:  Front Neurol       Date:  2020-10-15       Impact factor: 4.003

5.  A novel nonsense CDK5RAP2 mutation in a Somali child with primary microcephaly and sensorineural hearing loss.

Authors:  Alistair T Pagnamenta; Jennie E Murray; Grace Yoon; Elham Sadighi Akha; Victoria Harrison; Louise S Bicknell; Kaseem Ajilogba; Helen Stewart; Usha Kini; Jenny C Taylor; David A Keays; Andrew P Jackson; Samantha J L Knight
Journal:  Am J Med Genet A       Date:  2012-08-10       Impact factor: 2.802

  5 in total

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