Histopathology of mitochondrial cytopathy and the Laurence-Moon-Biedl syndrome

Clinical and histopathological studies of two patients with distinctly different inherited juvenile retinal dystrophies indicate that the ocular defect in mitochondrial cytopathy involves the underlying pigment epithelium, whereas in the Laurence-Moon-Biedl syndrome the photoreceptor cells are prima...

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Veröffentlicht in:British journal of ophthalmology 1986-10, Vol.70 (10), p.782-796
Hauptverfasser: Runge, P, Calver, D, Marshall, J, Taylor, D
Format: Artikel
Sprache:eng
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Zusammenfassung:Clinical and histopathological studies of two patients with distinctly different inherited juvenile retinal dystrophies indicate that the ocular defect in mitochondrial cytopathy involves the underlying pigment epithelium, whereas in the Laurence-Moon-Biedl syndrome the photoreceptor cells are primarily affected.
ISSN:0007-1161
1468-2079
DOI:10.1136/bjo.70.10.782