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Query: UMLS:C0025362 (mental retardation)
 15,878 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

We often experience the case that is difficult to differentiate normal from abnormal myelinating process by CT scan, because the diagnosis of myelinating maturation of the infant during developmental process is confusing. We can understand maturation of myelination adding to the advancement of diagnostic resolution by MR imager. So we obtain more informations about the abnormality of myelination and development of the brain by MR imaging than CT scan. This study demonstrates the ability of MR imaging to show progression of myelination in 10 infants and children. We also reveals the patients with disorders of neuronal migration or myelination during developing process. MR scanning could be obtained by sedation using such as triclofos or chloral hydrate for infant and younger children. It was necessary to use diazepam or pentazocine intravenously for elder children with mental retardation or restlessness. MR scans were performed with Siemens MAGNETOM 1.5 Tesla. T 1-weighted spin echo image (TR 600/TE 15) and T 2-weighted image (TR 3000/TE 90) were obtained for all cases. The ten normal infants and children (7 boys, 3 girls) were aged from 1 month to 4 years. Maturation of white matter generally proceeded from posterior limb of internal capsule to middle cerebellar peduncle, cerebellar white matter, corpus callosum, anterior limb of internal capsule, occipital white matter, centrum semiovale, finally frontal white matter. Myelination was matured during the first two years by T 2-weighted images. Changes caused by brain myelination were seen earlier on T 1-weighted images (7 months after birth) than on T 2-weighted images (one year and 9 months after birth).(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:[The MR evaluation of normal children and disorders of neuronal migration and myelination]. 235 20

We report a 10-year-old boy with chronic enteroviral meningitis associated with agammaglobulinemia (CEMA) and hydrocephalus. He was treated with a low-dose intravenous administration (100 mg/kg/4 weeks) of gammaglobulin (gamma-gl) since he was diagnosed as having Bruton type agammaglobulinemia at 1 year of age. At this admission, neurological examination revealed meningeal signs, Babinski sign, frontal signs, urinary incontinence, and mental retardation (IQ = 48) which was considered to be a sequela of the enteroviral encephalitis which had occurred in his first year of life. T 1-weighted MR imaging of the brain following gadolinium administration revealed a marked dilatation of the lateral ventricles and dense enhancement of the meninges. Enterovirus was detected in the cerebrospinal fluid (CSF) using tissue culture. Histological examination of a biopsied leptomeningeal specimen revealed inflammatory thickening, which was a likely cause of the obstruction to the flow of CSF. The hydrocephalus in this patient was treated with external drainage of CSF from the lateral ventricle. The CEMA was brought into remission by means of the intraventricular administration of gamma-gl, at a dose of 125-250 mg/week (total dose: 1.5 g/8 weeks), in addition to the high dose intravenous administration (400 mg/kg/4 weeks) of gamma-gl. Because of the poor prognosis of patients with CEMA, the intraventricular administration of gamma-gl should be initiated immediately following a diagnosis of enteroviral meningitis.
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PMID:[A case of chronic enteroviral meningitis and hydrocephalus associated with Bruton type agammaglobulinemia]. 951 11