Severe myelinopathy in 49,XXXXY syndrome

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.

[1]  A. Gropman,et al.  Neurocognitive variance and neurological underpinnings of the X and Y chromosomal variations , 2013, American journal of medical genetics. Part C, Seminars in medical genetics.

[2]  J. Giedd,et al.  Brain morphological abnormalities in 49,XXXXY syndrome: A pediatric magnetic resonance imaging study☆☆☆ , 2013, NeuroImage: Clinical.

[3]  B. Tabarki,et al.  Further Magnetic Resonance Imaging (MRI) Brain Delineation of 49,XXXXY Syndrome , 2012, Journal of child neurology.

[4]  A. Gropman,et al.  Effects of short‐course androgen therapy on the neurodevelopmental profile of infants and children with 49,XXXXY syndrome , 2011, Acta paediatrica.

[5]  P. Zeitler,et al.  48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome , 2011, Acta paediatrica.

[6]  A. Vossough,et al.  Brain magnetic resonance imaging findings in 49,XXXXY syndrome. , 2008, Pediatric neurology.

[7]  J. Graham,et al.  Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY , 2007, American journal of medical genetics. Part A.

[8]  Dongmin Kim,et al.  49,XXXXY Syndrome with Diabetes Mellitus , 2006, Hormone Research in Paediatrics.

[9]  M. Baquero,et al.  White matter alterations associated with chromosomal disorders , 2004, Developmental medicine and child neurology.

[10]  P. Curatolo,et al.  Neurologic Aspects of 49,XXXXY Syndrome , 2003, Journal of child neurology.

[11]  A. Robinson,et al.  Sex chromosome tetrasomy and pentasomy. , 1995, Pediatrics.

[12]  A. Neuhold,et al.  Hypoplasia of the corpus callosum and growth hormone deficiency in the XXXXY syndrome. , 1992, American journal of medical genetics.