Wiskott-Aldrich syndrome in a female with skewed X-chromosome inactivation

Nuria Andreu, Núria Pujol-Moix, Luis Martinez-Lostao, Marta Oset, Eduardo Muñiz-Diaz, Xavier P. Estivill, Victor Volpini, Cristina Fillat

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

Wiskott-Aldrich syndrome (WAS) is an X-linked recessive disorder characterized by immunodeficiency, eczema, and thrombocytopenia with small platelets. The phenotype of affected males is usually severe, although female carriers of the disorder have no clinical signs of the genetic defect. This is explained by the preferential selection of the normal, nonmutated X-chromosome, as the active allele in hematopoietic cells. In the present article we describe a female case of WAS, with a G-to-A transition in the WASP gene at nucleotide 291. She displays mild thrombocytopenia, with both normal and small-sized platelets. A methylation analysis of the HUMARA gene showed a nonrandom X-chromosome inactivation pattern in which the X-chromosome carrying the normal WASP gene was preferentially inactivated, leaving the mutant gene active. Thus, our results suggest that skewed X-inactivation, favoring the WASP-mutated allele, is the mechanism underlying the WAS phenotype of this girl. Moreover the results alert us to the fact that particular females, with a family history of WAS, may develop certain signs of the disease.

Original languageEnglish
Pages (from-to)332-337
Number of pages6
JournalBlood Cells, Molecules, and Diseases
Volume31
Issue number3
DOIs
Publication statusPublished - Nov 2003
Externally publishedYes

Fingerprint

Wiskott-Aldrich Syndrome
X Chromosome Inactivation
X Chromosome
Thrombocytopenia
Genes
Blood Platelets
Alleles
Phenotype
Eczema
Methylation
Nucleotides

Keywords

  • Carrier
  • Platelets
  • Skewed X-chromosome inactivation
  • Thrombocytopenia
  • Wiskott-Aldrich syndrome

ASJC Scopus subject areas

  • Molecular Biology
  • Molecular Medicine
  • Hematology

Cite this

Andreu, N., Pujol-Moix, N., Martinez-Lostao, L., Oset, M., Muñiz-Diaz, E., Estivill, X. P., ... Fillat, C. (2003). Wiskott-Aldrich syndrome in a female with skewed X-chromosome inactivation. Blood Cells, Molecules, and Diseases, 31(3), 332-337. https://doi.org/10.1016/S1079-9796(03)00168-2

Wiskott-Aldrich syndrome in a female with skewed X-chromosome inactivation. / Andreu, Nuria; Pujol-Moix, Núria; Martinez-Lostao, Luis; Oset, Marta; Muñiz-Diaz, Eduardo; Estivill, Xavier P.; Volpini, Victor; Fillat, Cristina.

In: Blood Cells, Molecules, and Diseases, Vol. 31, No. 3, 11.2003, p. 332-337.

Research output: Contribution to journalArticle

Andreu, N, Pujol-Moix, N, Martinez-Lostao, L, Oset, M, Muñiz-Diaz, E, Estivill, XP, Volpini, V & Fillat, C 2003, 'Wiskott-Aldrich syndrome in a female with skewed X-chromosome inactivation', Blood Cells, Molecules, and Diseases, vol. 31, no. 3, pp. 332-337. https://doi.org/10.1016/S1079-9796(03)00168-2
Andreu, Nuria ; Pujol-Moix, Núria ; Martinez-Lostao, Luis ; Oset, Marta ; Muñiz-Diaz, Eduardo ; Estivill, Xavier P. ; Volpini, Victor ; Fillat, Cristina. / Wiskott-Aldrich syndrome in a female with skewed X-chromosome inactivation. In: Blood Cells, Molecules, and Diseases. 2003 ; Vol. 31, No. 3. pp. 332-337.
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