Literature DB >> 23359596

Musculoskeletal anomalies in a large cohort of boys with 49, XXXXY.

Courtney Sprouse1, Laura Tosi, Emily Stapleton, Andrea L Gropman, Francie L Mitchell, Rick Peret, Teresa Sadeghin, Kathryn Haskell, Carole A Samango-Sprouse.   

Abstract

49, XXXXY is a rare aneuploidy and variant of Klinefelter syndrome, occurring in 1 per 80,000-100,000 live births. We present a cohort of 40 affected males, focusing on musculoskeletal problems. Subjects were participants in an annual 49er family support group meeting. Children were examined in a multidisciplinary clinic by a pediatric neurologist and geneticist, a pediatric orthopedist, a neurodevelopmentalist, and two physical therapists. The patient data were collected from this clinic from 2004 to 2012. All patients were required to have karyotypes that confirmed the presence of XXXXY. There was a high prevalence of musculoskeletal disorders, particularly hypotonia (34 patients [85%]), radioulnar synostosis (30 [75%]), pes planus (26 [65%]), asymmetric hip rotation (27 [67.5%]), and clinodactyly (24 [60%]). Other, less common lower-extremity disorders, included, 5 patients (12.5%) with unilateral club foot, 5 boys (12.5%) with pes cavus, 10 patients (25%) genu valgum and 2 children with genu varus (5%). To our knowledge, this is the first large cohort of boys with 49, XXXXY that focuses on musculoskeletal disorders. There was an increased incidence of hypotonia, clubfoot, avascular necrosis of the femoral head, radioulnar synostosis, and pes planus compared to the normative population. Boys with 49, XXXXY would benefit from multidisciplinary evaluations, particularly from pediatric orthopedists, physical therapists, neurologists, and geneticists for appropriate medical care.
Copyright © 2013 Wiley Periodicals, Inc.

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Year:  2013        PMID: 23359596     DOI: 10.1002/ajmg.c.31354

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  7 in total

Review 1.  Leydig cell tumor in a patient with 49,XXXXY karyotype: a review of literature.

Authors:  Salwan Maqdasy; Laura Bogenmann; Marie Batisse-Lignier; Béatrice Roche; Fréderic Franck; Françoise Desbiez; Igor Tauveron
Journal:  Reprod Biol Endocrinol       Date:  2015-07-10       Impact factor: 5.211

2.  Neonatal diagnosis of 49, XXXXY syndrome.

Authors:  Katayoon Etemadi; Behnaz Basir; Safieh Ghahremani
Journal:  Iran J Reprod Med       Date:  2015-03

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

4.  Effects of sex chromosome dosage on corpus callosum morphology in supernumerary sex chromosome aneuploidies.

Authors:  Benjamin S C Wade; Shantanu H Joshi; Martin Reuter; Jonathan D Blumenthal; Arthur W Toga; Paul M Thompson; Jay N Giedd
Journal:  Biol Sex Differ       Date:  2014-10-16       Impact factor: 5.027

5.  Treatment of genu valgum in children by means of temporary hemiepiphysiodesis using eight-plates: short-term findings.

Authors:  Dirk Zajonz; Eckehard Schumann; Magdalena Wojan; Fabian B Kübler; Christoph Josten; Ulf Bühligen; Christoph E Heyde
Journal:  BMC Musculoskelet Disord       Date:  2017-11-15       Impact factor: 2.362

6.  A rare 47 XXY/46 XX mosaicism with clinical features of Klinefelter syndrome.

Authors:  Noor Shafina Mohd Nor; Muhammad Yazid Jalaludin
Journal:  Int J Pediatr Endocrinol       Date:  2016-06-02

7.  Testosterone replacement in 49,XXXXY syndrome: andrological, metabolic and neurological aspects.

Authors:  Rossella Mazzilli; Michele Delfino; Jlenia Elia; Francesco Benedetti; Laura Alesi; Luciana Chessa; Fernando Mazzilli
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2015-12-23
  7 in total

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