
Includes congenital malformations, lipidoses, leucodystrophies and demylelinating disorders, the ataxias and familial spastic paraplegia, spinal muscular atrophies and related disorders, paralysis agitans and disorders of the basal ganglia, pre-senile and senial dementias, disorders of the cranial and peripheral nerves and sensory syndromes, neoplasms and related disorders, epilepsies and related disorders, miscellaneous disorders, higher level disorders, disorders of intermediary metabolism, disorders of muscle, a bibliography, and an index.
This monograph investigates the hereditary patterns and clinical manifestations of a wide range of neurological disorders. R.T.C. Pratt provides a systematic overview of genetic influences on nervous system pathology, drawing upon clinical observations and familial data available at the time of publication. The text serves as a structured reference for understanding the intersection of genetic inheritance and neurological dysfunction.
What You Will Find
Scope Limits
Experts recognize this work as a foundational reference for the historical study of medical genetics in neurology. Readers frequently note the clinical density of the prose, which provides a comprehensive overview of hereditary neurological conditions.
Page Count:
318
Publication Date:
1967-01-01
Publisher:
Oxford University Press
ISBN-10:
0192641298
ISBN-13:
9780192641298
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