Developmental neuropathology /
This book presents for the first time a dual approach to the wide range of disorders which affect the developing brain in pre- and post-natal life, stressing the genetic and molecular mechanisms but recognizing the practicing neuropathologist and pediatric pathologist need cogent and logical guidanc...
| Other Authors: | , |
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| Format: | Book |
| Language: | English |
| Published: |
Basel, Switzerland :
ISN Neuropath Press,
[2004]
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| Series: | Pathology & genetics.
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| Subjects: |
Table of Contents:
- Forebrain patterning defects
- Neural tube defects
- Midline patterning defects
- Microcephaly
- Cell migration and specification disorders
- Lissencephaly, type I
- Lissencephaly, type II (Cobblestone)
- Polymicrogyria
- Cerebral heterotopia
- Epilepsy part I : cortical dysplasia
- Epilepsy part I : hemimegalencephaly
- Epilepsy part II : rasmussen syndrome, hippocampal sclerosis, granule cell dysplasia
- Tuberous sclerosis
- Cerebellum, hindbrain, and spinal patterning defects
- Chiari malformations
- Dandy walker malformation
- Cerebellar heterotopia and dysplasia
- Brainstem malformations
- Spinal cord lesions
- Anomalies of cerebral vasculature
- Pediatric vascular malformations
- Hydrocephalus
- Hydrocephalus
- Secondary malformations and destructive pathologies
- Disruptions of development
- Antenatal disruptive lesions
- Specific destructive disorders
- Hemorrhagic lesions
- White matter lesions in the perinatal period
- Grey matter lesions
- Acquired vascular lesions in children
- Pediatric head injury
- SIDS
- Sudden infant death syndrome
- Metabolic and exogenous toxins
- Kernicterus
- Lesions induced by toxins
- Metabolic disorders
- Disorders of carbohydrate metabolism, introduction and lysosomal disorders
- Disorders of carbohydrate metabolism. polyglucosan disorders.
- Disorders of carbohydrate metabolism. The congenital disorders of glycoslation.
- Sphinogolipidoses
- GM1 gangliosidosis
- GM2 gangliosidosis
- Niemann-pick disease types A and B
- Gaucher disease
- Farber disease
- Fabry disease
- Metachromatic leukodystrophy
- Multiple sulfatase deficiency
- Globoid cell leukodystrophy
- Sphingolipid activator protein defiency
- The neuronal ceroid lipofuscinoses
- Palmitoyl-protein thioesterase 1 deficiency with granular osmiophilic deposits (CLN1)
- Classic late-infantile NCL with tripeptidyl-peptidase I deficiency (CLN2)
- Juvenile NCL with mutations in CLN3 gene (CLN3)
- Rare forms of neuronal ceroid lipofuscinoses
- Niemann-pick type C disease
- Peroxisomal disorders
- Mitochondrial disorders
- Disorders of amino acid metabolism
- Pelizaeus- Merzbacher disease
- Cockayne syndrome
- Vanishing white matter disease
- Alexander disease
- Infantile neuroaxonal dystrophy (Seitilberger disease)
- Neurodegeneration with brain iron accumulation type 1
- Spinal muscular atrophy
- Neuropathology of autism
- Rett syndrome
- Infectious diseases
- Intrauterine infections
- Perinatal and postnatal infections