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Alterations of the Cerebral White Matter in a Middle-Aged Patient with Turner Syndrome: An MRI StudyTanji H.a · Nakajima K.b · Wada M.a · Kato T.a
aDepartment of Neurology, Hematology, Metabolism, Endocrinology and Diabetology (DNHMED), Yamagata University School of Medicine, and bDepartment of Internal Medicine, Tendo City Hospital, Yamagata, Japan Corresponding Author
Haruko Tanji, MD
Department of Neurology, Hematology, Metabolism, Endocrinology and
Diabetology (DNHMED), Yamagata University School of Medicine2-2-2 Iida-Nishi, Yamagata 990-9585 (Japan)
Tel. +81 23 628 5316, E-Mail firstname.lastname@example.org
A 52-year-old woman with intellectual disability was admitted to the hospital due to pneumonia. MRI of her brain showed diffuse hyperintensities on T2-weighted and fluid attenuated inversion recovery images in the bilateral cerebral white matter. Laboratory examination revealed sustained high levels of serum KL-6. Karyotyping revealed partial monosomy of the X chromosome. This is the first case showing diffuse white matter lesions in the brain, and sustained high levels of serum KL-6 in Turner syndrome.
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