Literature DB >> 14659786

Two 48,XXYY patients: clinical, cytogenetic and molecular aspects.

L Zelante1, M R Piemontese, G Francioli, S Calvano.   

Abstract

Two 48,XXYY males, a young and an adult patient, have been clinically and molecularly analysed. Clinical findings seem less severe in the young patient. This clinical difference could be mainly due to the age of the younger patient or, alternatively, the different pattern of X-inactivation observed in the two patients could play a role in the degree of the clinical manifestations.

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Year:  2003        PMID: 14659786     DOI: 10.1016/s0003-3995(03)00030-3

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  6 in total

1.  48,XXYY in a General Adult Psychiatry Department.

Authors:  Nuno Borja-Santos; Bruno Trancas; Pilar Santos Pinto; Bárbara Lopes; António Gamito; Sandra Almeida; Berta Ferreira; Antonio Luengo; Carlos Vieira; Jorge Martinho; Bruno Pereira; Graça Cardoso
Journal:  Psychiatry (Edgmont)       Date:  2010-03

2.  A rare sex chromosome aneuploidy: 48,XXYY syndrome.

Authors:  Tahir Atik; Özgür Çoğulu; Ferda Özkınay
Journal:  Turk Pediatri Ars       Date:  2016-06-01

Review 3.  48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome.

Authors:  Nicole Tartaglia; Natalie Ayari; Susan Howell; Cheryl D'Epagnier; Philip Zeitler
Journal:  Acta Paediatr       Date:  2011-04-08       Impact factor: 2.299

4.  A new look at XXYY syndrome: medical and psychological features.

Authors:  Nicole Tartaglia; Shanlee Davis; Alison Hench; Sheela Nimishakavi; Renee Beauregard; Ann Reynolds; Laura Fenton; Lindsey Albrecht; Judith Ross; Jeannie Visootsak; Robin Hansen; Randi Hagerman
Journal:  Am J Med Genet A       Date:  2008-06-15       Impact factor: 2.802

5.  48XXYY Syndrome in an Adult with Type 2 Diabetes Mellitus, Unilateral Renal Aplasia, and Pigmentary Retinitis.

Authors:  Baha Zantour; Mohamed Habib Sfar; Samia Younes; Wafa Alaya; Mahdi Kamoun; Emna Mkaouar; Saida Jerbi
Journal:  Case Rep Med       Date:  2010-08-17

6.  A new 48, XXYY/47, XYY syndrome associated with multiple skeletal abnormalities, congenital heart disease and mental retardation.

Authors:  Leon Mutesa; Mauricette Jamar; Anne Cecile Hellin; Genevieve Pierquin; Vincent Bours
Journal:  Indian J Hum Genet       Date:  2012-09
  6 in total

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