Literature DB >> 19817277

Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes.

Pelin Ozlem Simşek1, Gülen Eda Utine, Ayfer Alikaşifoğlu, Yasemin Alanay, Koray Boduroğlu, Nurgün Kandemir.   

Abstract

49,XXXXY and 48,XXXY syndromes are rare gonosomal aneuploidies in which the affected individuals present with characteristic facial and skeletal malformations, intrauterine growth retardation, and psychomotor retardation. Psychological, endocrinologic and orthopedic disorders constitute the major problems in the clinical follow-up. Sex chromosome abnormalities should especially be kept in mind in the evaluation of patients with micropenis, mental retardation and accompanying behavioral disturbances. Management mandates a multidisciplinary approach with pediatric endocrinology, pediatric surgery, orthopedics, psychiatry, and clinical genetic evaluations.

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Year:  2009        PMID: 19817277

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  3 in total

Review 1.  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

2.  Cytogenetic status of patients with congenital malformations or suspected chromosomal abnormalities in Turkey: a comprehensive cytogenetic survey of 11,420 patients.

Authors:  Osman Demirhan; Erdal Tunç
Journal:  Chromosoma       Date:  2022-10-11       Impact factor: 2.919

3.  48, XXXY/49, XXXXY mosaic: new neuroradiological features in an ultra-rare syndrome.

Authors:  Donatella Milani; Francesca Bonarrigo; Sabrina Avignone; Fabio Triulzi; Susanna Esposito
Journal:  Ital J Pediatr       Date:  2015-07-14       Impact factor: 2.638

  3 in total

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