Titlebook: Magnetic Resonance of Myelin, Myelination and Myelin Disorders; Marjo S. Knaap,Jacob Valk Book 19952nd edition Springer-Verlag Berlin Heid

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Multiple Sulfatase Deficiency,hromatic leukodystrophy and mucopolysaccharidosis. It is also called mucosulfatidosis, Austin’s variant or variant O. Three different types of MSD have been described: a neonatal form, an early-childhood form and a very rare juvenile form.

FAST

,Globoid Cell Leukodystrophy: Krabbe’s Disease,f clinical types can be distinguished, which differ in age of onset and in the more or less rapid course of symptomatology. The early-infantile type or classical type is most well known. The other types are: congenital, lateinfantile, juvenile and adolescent-adult. Early and late onset forms of GLD may occur within the same family.

preeclampsia

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Mucopolysaccharidoses, of mucopolysaccharides (glycosaminoglycans). The MPS are classified into six groups, which are further subdivided on the basis of genetic, biochemical and clinical findings (Table 13.1). These disorders share a number of characteristic clinical features, although there is considerable variability among the MPS types and within one type of MPS.

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撕裂皮肉

crumble

amplitude

Classification of Myelin Disorders,The history of classifications of myelin disorders shows how each classification reflects the state of scientific development of its time. Based on recent scientific insights, a revised classification is proposed at the end of this chapter.

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