Literature DB >> 7246603

Pentasomy X: report of patient and studies of X-inactivation.

S J Funderburk, M Valente, I Klisak.   

Abstract

A five-year-old girl presented with mental retardation (MR), microcephaly, short stature, ptosis, malocclusion, abnormal elbows, fifth finger clinodactyly, joint hyperextensibility in hands and feet, renal hypoplasia, nonobstructive ureteral stasis, pyelonephritis, and renal failure. Five X chromosomes (49,XXXXX) were found in all peripheral blood lymphocytes and skin fibroblasts examined. Xa RBC typing, utilizing serial dilutions of antiserum, gave agglutination at a higher titer than in either Xg(a+) positive parent; the patient's serum IgM was also elevated. These immunological findings imply a lack of dosage compensation and incomplete inactivation of some X-linked loci.

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Year:  1981        PMID: 7246603     DOI: 10.1002/ajmg.1320080105

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


  2 in total

1.  A new case of prenatally diagnosed pentasomy x: review of the literature.

Authors:  Linda Maria Azzurra Pirollo; Leila Baghernajad Salehi; Simona Sarta; Marco Cassone; Maria Vittoria Capogna; Emilio Piccione; Giuseppe Novelli; Adalgisa Pietropolli
Journal:  Case Rep Obstet Gynecol       Date:  2015-01-29

2.  Detailed analysis of X chromosome inactivation in a 49,XXXXX pentasomy.

Authors:  Lucia M Moraes; Leila Ca Cardoso; Vera Ls Moura; Miguel Am Moreira; Albert N Menezes; Juan C Llerena; Héctor N Seuánez
Journal:  Mol Cytogenet       Date:  2009-10-07       Impact factor: 2.009

  2 in total

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