4 results match your criteria: "Yokohama Ryo-iku Medical Center.[Affiliation]"
Brain Dev
January 2006
Department of Pediatrics and Pediatric Neurology, Yokohama Ryo-iku Medical Center, Yokohama 241-0014, Japan.
Pallister-Killian syndrome (PKS) is a disorder caused by a mosaic tetrasomy of chromosome 12p, which manifests with dysmorphism, intellectual disabilities, auditory disturbance, and epilepsy. Here, we describe the findings of brain magnetic resonance (MR) imaging in two patients with PKS. One patient, a 43-year-old man, showed multiple lesions with high signal intensity on T2-weighted image (WI) in the basal ganglia, and widespread T2 elongation in the periventricular white matter.
View Article and Find Full Text PDFActa Neuropathol
July 2005
Department of Pediatrics and Pediatric Neurology, Yokohama Ryo-iku Medical Center, Asahi-ku, Japan.
We report the autopsy case of a 40-year-old woman with severe intellectual and motor disabilities, who showed calcification in the cerebellum and pons but not in the basal ganglia on CT scan, and died of intracranial hemorrhage due to intractable hypertension. At autopsy, numerous calcium deposits were noted in the cerebellar cortex, the dentate nucleus, the cerebellar white matter and the ventral pons. These deposits were distributed both in the neuropil and the white matter, but rarely within the arterial walls or in contact with capillaries.
View Article and Find Full Text PDFBrain Dev
December 2005
Department of Pediatrics and Pediatric Neurology, Yokohama Ryo-iku Medical Center, 557-2 Ichizawa-cho, Asahi-ku, Yokohama, and Department of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.
We report on three patients with xeroderma pigmentosum group A (XPA) who showed laryngeal stridor in their 20s. The stridor appeared on feeding and emotional excitation, was exaggerated during respiratory infection and was life-threatening on some occasions. Adduction of the vocal cords during inspiration, observed by laryngoscopy, confirmed laryngeal dystonia in all cases.
View Article and Find Full Text PDFRinsho Shinkeigaku
March 2005
Department of Pediatrics and Pediatric Neurology, Yokohama Ryo-iku Medical Center.
We reported a 36-year-old man, who suffered from cluster headache (CH) associated with hemicrania continua (HC). The continuous, dull or pressure-type headache appeared on the same side of the CH during the third month of a prolonged cluster period, and fluctuated in the severity of pain. This headache was aggravated when the CH was ameliorated by the administration of lithium carbonate.
View Article and Find Full Text PDF