Literature DB >> 21590264

Tetrasomy and pentasomy of the X chromosome.

Edith Schoubben1, Karin Decaestecker, Koen Quaegebeur, Lode Danneels, Geert Mortier, Luc Cornette.   

Abstract

UNLABELLED: We describe a newborn girl with a life-threatening laryngomalacia and extreme hypotonia. Genetic analysis revealed the very rare genetic condition mosaicism of 48,XXXX and 49,XXXXX (50/50). We here state that the degree of early hypotonia constitutes an important early prognostic feature in this syndrome. The timely insertion of a gastrostomy is warranted in order to prevent aspiration.
CONCLUSION: A karyotype is mandatory in female newborns with moderate to severe hypotonia in order to exclude polyploid mosaicism of the X chromosome. An 'overall prognosis' for 48,XXXX and 49,XXXXX girls is difficult to provide towards parents in line with a well-known, substantial variability in outcome for all polysomy X infants.

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Year:  2011        PMID: 21590264     DOI: 10.1007/s00431-011-1491-9

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  5 in total

1.  A PHENOTYPIC FEMALE WITH 49 CHROMOSOMES, PRESUMABLY XXXXX. A CASE REPORT.

Authors:  N KESAREE; P V WOOLLEY
Journal:  J Pediatr       Date:  1963-12       Impact factor: 4.406

2.  An XXXX sex chromosome complex in two mentally defective females.

Authors:  D H CARR; M L BARR; E R PLUNKETT
Journal:  Can Med Assoc J       Date:  1961-01-21       Impact factor: 8.262

3.  Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis.

Authors:  Faustina Lalatta; Donatella Quagliarini; Emanuela Folliero; Ugo Cavallari; Barbara Gentilin; Pierangela Castorina; Francesca Forzano; Serena Forzano; Enrico Grosso; Valeria Viassolo; Valeria Giorgia Naretto; Stefania Gattone; Florinda Ceriani; Francesca Faravelli; Luigi Gargantini
Journal:  Eur J Pediatr       Date:  2010-05-15       Impact factor: 3.183

4.  48,XXXX-49,XXXXX mosaic: asynchronies among the late-replicating X chromosomes.

Authors:  N Ricci; B Dallapiccola; B Ventimiglia; L Tiepolo; M Fraccaro
Journal:  Cytogenetics       Date:  1968

Review 5.  Sex chromosome tetrasomy and pentasomy.

Authors:  M G Linden; B G Bender; A Robinson
Journal:  Pediatrics       Date:  1995-10       Impact factor: 7.124

  5 in total
  5 in total

1.  Unusual brain changes in tetrasomy x chromosomal anomaly.

Authors:  M Mshelbwala; P Venugopalan
Journal:  Sultan Qaboos Univ Med J       Date:  2012-11-20

2.  Experiences of individuals receiving a sex chromosome multisomy diagnosis.

Authors:  Jordan P Richardson; Nivedita Ahlawat; Kirsten A Riggan; Sharron Close; Megan A Allyse
Journal:  J Community Genet       Date:  2022-08-19

3.  Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child.

Authors:  Kirsten A Riggan; Sharron Close; Megan A Allyse
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-03-17       Impact factor: 3.908

4.  Report of a new case with pentasomy X and novel clinical findings.

Authors:  O Demirhan; N Tanriverdi; M B Yilmaz; S Kocaturk-Sel; N Inandiklioglu; U Luleyap; E Akbal; G Comertpay; T Tufan; O Dur
Journal:  Balkan J Med Genet       Date:  2015-12-30       Impact factor: 0.519

5.  A case of penta X syndrome caused by nondisjunction in maternal meiosis 1 and 2.

Authors:  Sara Markholt; Jesper Graakjaer; Signe Bødker Thim; Bente Høst; Anne-Bine Skytte
Journal:  Clin Case Rep       Date:  2017-06-01
  5 in total

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