Literature DB >> 28627968

Severe myelinopathy in 49,XXXXY syndrome.

Mark A Buller1, Cory M Pfeifer2.   

Abstract

49,XXXXY is a rare aneuploidy with neuroanatomic findings scarcely reported in the literature. Given the fact that many of its phenotypic characteristics are similar to Klinefelter patients, 49,XXXXY has been treated as a variant of Klinefelter syndrome in the past. Newer studies have shown that intellectual disabilities and cardiac sequelae are more common in 49,XXXXY making the need for more precise characterization of the disorder essential. Prior case studies have demonstrated focal (and to a lesser extent confluent) white abnormalities as well as enlarged perivascular cysts (often in clustered arrangements) in the brains of these patients, but high resolution magnetic resonance images of severe myelinopathy are infrequently documented. Presented here is an exceptional manifestation of this rare disease with substantial findings in the brain exhibiting both confluent white matter changes and diffuse perivascular cysts. Cases such as this one serve to expand the differential considerations for confluent dysmyelinating disease and improve diagnostic efficacy.

Entities:  

Keywords:  49; XXXXY; myelinopathy; perivascular cysts

Mesh:

Year:  2017        PMID: 28627968      PMCID: PMC6136133          DOI: 10.1177/1971400917703989

Source DB:  PubMed          Journal:  Neuroradiol J        ISSN: 1971-4009


  12 in total

Review 1.  Neurocognitive variance and neurological underpinnings of the X and Y chromosomal variations.

Authors:  Andrea Gropman; Carole A Samango-Sprouse
Journal:  Am J Med Genet C Semin Med Genet       Date:  2013-01-18       Impact factor: 3.908

Review 2.  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

Review 3.  Sex chromosome tetrasomy and pentasomy.

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

4.  Effects of short-course androgen therapy on the neurodevelopmental profile of infants and children with 49,XXXXY syndrome.

Authors:  Carole A Samango-Sprouse; Andrea L Gropman; Teresa Sadeghin; Madison Kingery; Margaret Lutz-Armstrong; Alan D Rogol
Journal:  Acta Paediatr       Date:  2011-04-20       Impact factor: 2.299

5.  Further magnetic resonance imaging (MRI) brain delineation of 49,XXXXY syndrome.

Authors:  Brahim Tabarki; Shatha Al Shafi; Nawal Al Adwani; Saad Al Shahwan
Journal:  J Child Neurol       Date:  2011-12-07       Impact factor: 1.987

6.  49,XXXXY syndrome with diabetes mellitus.

Authors:  Hee Jin Kim; Dongmin Kim; Jae Min Shin; Hyun-Kyung Chung; Gilho Lee
Journal:  Horm Res       Date:  2005-12-15

7.  Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY.

Authors:  Jeannie Visootsak; Beth Rosner; Elisabeth Dykens; Nicole Tartaglia; John M Graham
Journal:  Am J Med Genet A       Date:  2007-06-01       Impact factor: 2.802

8.  Hypoplasia of the corpus callosum and growth hormone deficiency in the XXXXY syndrome.

Authors:  G Haeusler; H Frisch; Z Guchev; F Hadziselimovic; A Neuhold; W Vormittag
Journal:  Am J Med Genet       Date:  1992-09-15

9.  White matter alterations associated with chromosomal disorders.

Authors:  Angels García-Cazorla; Anna Sans; Miguel Baquero; María Dolores García-Bargo; Montse Arellano; Pilar Poo; Esther Gean; Jaume Campistol
Journal:  Dev Med Child Neurol       Date:  2004-03       Impact factor: 5.449

10.  Brain morphological abnormalities in 49,XXXXY syndrome: A pediatric magnetic resonance imaging study.

Authors:  Jonathan D Blumenthal; Eva H Baker; Nancy Raitano Lee; Benjamin Wade; Liv S Clasen; Rhoshel K Lenroot; Jay N Giedd
Journal:  Neuroimage Clin       Date:  2013       Impact factor: 4.881

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