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Familial amaurotic idiocy and Neimann-Pick disease for comparison. Familial cerebro-macular degeneration and familial retinal degeneration--'retinal aliotrophy'

Date
1903-1951
Reference
PP/FPW/B.115
Part of
Parkes Weber, Frederick (1863-1962)
  • Archives and manuscripts

About this work

Description

Allied forms of cereberal diplegia and progressive cerebellar ataxia. Megalencephaly, hypertrophic cerebral sclerosis and atrophic cerebral scelerosis ('walnut brain'). Cerebral degeneration. Familial occurrence of hydrocephalus internus. Various forms of night-blindness and retinitis pigmentosa, with or without cerebral degeneration or epileptiform fits. 'Lawrence-Moon-Biedl syndrome' etc. Congenital cerebral cortical blindness etc (to compare' 'Dnasen'. 'Holes in the Macula'. 'An undescribed familial parathyroid syndrome in ionfants'. Allureal pigmentary sundrome. Acoustico-retino-cerebrospinal hereditary diseases (K[....] t-H[..]mmers of [....]). 'Optico-cochlio-dentelic degeneration'. Hereditary Optic Atrophy (Lebers[....)]

Publication/Creation

1903-1951

Physical description

1 file

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