Literature DB >> 31602194

Copy Number Gain at Xq28 in a Child with Global Developmental Delay Associated with a Variant Form of Hoyeraal-Hreidarsson Syndrome.

Lélia L Gonçalves Ramos1,2, Irene Plaza Pinto2,3, Rajib Deb2,4, Cristiano L Ribeiro2,3, Damiana Mírian da Cruz E Cunha2, Lysa Bernardes Minasi2,5, Antonio M T Cordeiro Silva1,6, Aparecido D da Cruz2,3,5,7.   

Abstract

We report the case of a child from Central Brazil with global developmental delay (GDD), syndromic features, and absence of abnormal skin pigmentation, nail dystrophy, and leukoplakia of the oral mucosa, with a rearrangement at Xq28 harboring the DKC1 gene. GTC-banding revealed a male karyotype (46,XY) with no visible numerical or structural alterations. Chromosomal microarray analysis (CMA) showed a 0.36-Mb gain at Xq28 of maternal origin, encompassing 22 genes, including DKC1. Rearrangements and mutations involving this gene have been associated with dyskeratosis congenita, X-linked (OMIM 305000) and Hoyeraal-Hreidarsson syndrome. CMA was a powerful and efficient approach to identify a gain at Xq28 harboring the DKC1 gene in our patient with GDD syndromic features and no cutaneous alterations, suggesting that this variant is associated with the Hoyeraal-Hreidarsson syndrome.
Copyright © 2019 by S. Karger AG, Basel.

Entities:  

Keywords:  Chromosomal microarray analysis; DKC1; Genetic syndrome; Global developmental delay

Year:  2019        PMID: 31602194      PMCID: PMC6738202          DOI: 10.1159/000500005

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN: 1661-8769


  14 in total

1.  Congenital hypoplastic thrombocytopenia and cerebral malformations in two brothers.

Authors:  H M Hoyeraal; J Lamvik; P J Moe
Journal:  Acta Paediatr Scand       Date:  1970-03

2.  Investigation of chromosome X inactivation and clinical phenotypes in female carriers of DKC1 mutations.

Authors:  Jialin Xu; Payal P Khincha; Neelam Giri; Blanche P Alter; Sharon A Savage; Judy M Y Wong
Journal:  Am J Hematol       Date:  2016-11-04       Impact factor: 10.047

3.  Mouse dyskerin mutations affect accumulation of telomerase RNA and small nucleolar RNA, telomerase activity, and ribosomal RNA processing.

Authors:  Yuko Mochizuki; Jun He; Shashikant Kulkarni; Monica Bessler; Philip J Mason
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-07       Impact factor: 11.205

4.  A pathogenic dyskerin mutation impairs proliferation and activates a DNA damage response independent of telomere length in mice.

Authors:  Bai-Wei Gu; Monica Bessler; Philip J Mason
Journal:  Proc Natl Acad Sci U S A       Date:  2008-07-14       Impact factor: 11.205

Review 5.  Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.

Authors:  N Hiroi; T Takahashi; A Hishimoto; T Izumi; S Boku; T Hiramoto
Journal:  Mol Psychiatry       Date:  2013-08-06       Impact factor: 15.992

6.  The Hoyeraal-Hreidarsson syndrome: the fourth case of a separate entity with prenatal growth retardation, progressive pancytopenia and cerebellar hypoplasia.

Authors:  C M Aalfs; H van den Berg; P G Barth; R C Hennekam
Journal:  Eur J Pediatr       Date:  1995-04       Impact factor: 3.183

7.  Hoyeraal-Hreidarsson Syndrome: An Extremely Rare Dyskeratosis Congenita Phenotype.

Authors:  Özgür Bakar; Ugˇur Işik; Cengiz Canpolat; Yasemin Alanay
Journal:  Pediatr Dermatol       Date:  2015-10-08       Impact factor: 1.588

8.  A syndrome of progressive pancytopenia with microcephaly, cerebellar hypoplasia and growth failure.

Authors:  S Hreidarsson; K Kristjansson; G Johannesson; J H Johannsson
Journal:  Acta Paediatr Scand       Date:  1988-09

9.  Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) gene.

Authors:  Jonathan K Alder; Erin M Parry; Srinivasan Yegnasubramanian; Christa L Wagner; Lawrence M Lieblich; Robert Auerbach; Arleen D Auerbach; Sarah J Wheelan; Mary Armanios
Journal:  Hum Mutat       Date:  2013-09-11       Impact factor: 4.878

Review 10.  Unraveling the pathogenesis of Hoyeraal-Hreidarsson syndrome, a complex telomere biology disorder.

Authors:  Galina Glousker; Fabien Touzot; Patrick Revy; Yehuda Tzfati; Sharon A Savage
Journal:  Br J Haematol       Date:  2015-05-04       Impact factor: 6.998

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