Causes of Dyslexia
Dyslexia Causes: Book Excerpts
Dyslexia as a symptom:
Conditions listing Dyslexia
as a symptom may also be potential underlying causes of Dyslexia.
Our database lists the following as having
Dyslexia as a symptom of that condition:
Medical news summaries relating to Dyslexia:
The following medical news items are relevant to causes of Dyslexia:
Related information on causes of Dyslexia:
As with all medical conditions,
there may be many causal factors.
Further relevant information on causes of Dyslexia may be found in:
Causes of Dyslexia: Online Medical Books
16 MEDICAL BOOKS ONLINE!
Review excerpts from medical books online, free, without registration,
for more information about the causes of Dyslexia.
Developmental Delay:
Principal Causes of Developmental Delay
(The Diagnostic Approach to Symptoms and Signs in Pediatrics)
- Grossmotor delay
- Cerebralpalsy
- Neuromuscular disorders
- Delayed or impaired language
- Impairedhearing
- Receptive and expressive language disorders
- Pervasive developmental disorders
- Static global delay
- Chromosomaldisturbances
- Maternal or infant undernutrition
- Maternal drug or alcohol use
- Cerebral malformation
- Hypoxic-ischemic encephalopathy
- Intracranial hemorrhage
- Infection
- Brain tumor
- Cerebrovascular disorders
- Psychologic disturbances
- Unknown
- Progressive global delay
- Neurocutaneousdisorders
- Tuberoussclerosis
- Neurofibromatosis
- Metabolic brain disorders
- Diseasesprimarily affecting gray matter (without visceral storage)
- GM-2 gangliosidosis(Tay-Sachs disease)
- Neuronal ceroid lipofuscinoses
- Alpers disease
- Menkes disease
- Rett syndrome
- Diseases primarily affecting gray matter(with visceral storage)
- GM-1 gangliosidosis
- GM-2 gangliosidosis (Sandhoff disease)
- Niemann-Pick disease
- Gaucher disease
- Fucosidosis
- Sialidosis type II
- Diseases primarily affecting whitematter
- Galactosemia
- Phenylketonuria
- Maple syrup urine disease (intermediate)
- Homocystinuria
- Urea cycle defects
- Canavan disease
- Alexander disease
- Globoid leukodystrophy (Krabbe disease)
- Pelizaeus-Merzbacher disease
- Metachromatic leukodystrophy
- Diseases affecting both gray and whitematter
- Mucopolysaccharidoses
- Mucopolysaccharidosistype I (Hurler disease)
- Mucopolysaccharidosis type II (Hunterdisease)
- Mucopolysaccharidosis type III (Sanfilippodisease)
- Mucopolysaccharidosis type VII (Slydisease)
- Mitochondrial disorders
- Peroxisomal disorders
- Miscellaneous
- Lesch-Nyhan syndrome
- Congenital hypothyroidism
- Human immunodeficiency virus infection
» READ BOOK EXCERPT ONLINE »
Source: The Diagnostic Approach to Symptoms and Signs in Pediatrics, 2006
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