Pigmentary degeneration of the retina in the Hallervorden-Spatz syndrome

American Journal of Ophthalmology

Volumn 88, Issue 3 PART 1, 1979, Pages 467-471

  Newell, Frank W ^a   Johnson II, Royce O ^a   Huttenlocher, Peter R ^a  

^a UNIVERSITY OF CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; DIZYGOTIC TWINS; HALLERVORDEN SPATZ DISEASE; HEREDITY; NERVOUS SYSTEM; TAPETORETINAL DEGENERATION; VISUAL SYSTEM;

BASAL GANGLIA DISEASES; CASE REPORT; CHILD; DISEASES IN TWINS; FEMALE; HALLERVORDEN-SPATZ SYNDROME; HUMAN; MALE; PIGMENT EPITHELIUM OF EYE; PREGNANCY; RETINAL DEGENERATION; TWINS, DIZYGOTIC;

EID: 0018320556     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/0002-9394(79)90648-2     Document Type: Article

References (14)

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5. Clinicopathological and histochemical studies of Hallervorden-Spatz disease with torsion dystonia with special reference to diagnostic criteria of the disease from the clinicopathological viewpoint
6. Dystrophie neuroaxonale et maladie de Hallervorden-Spatz infantiles. Aspects électrocliniques et anatomopathologiques, diagnostic differentiel
7. Coexistence of Hallervorden-Spatz disease with acanthocytosis
8. Contribution à l'étude des syndromes du globe pale. La dégénérescence progressive du globe pale et de la portion réticulée de la substance noire
9. Die Hallervorden-Spatsche Krankheit
10. Dégénérescence spongieuse juvénile du système nerveux central
11. Pigmentary retinal dystrophy in Hallervorden-Spatz disease. Clinicopathological report of a case
12. Hallervordenova-Spatzova pigmentová degenerace palida
13. An autopsy case of Hallervorden-Spatz disease. Clinicopathological and biochemical study
14. Hallervorden-Spatz syndrome