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
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container_title British journal of ophthalmology
container_volume 70
creator Runge, P
Calver, D
Marshall, J
Taylor, D
description 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.
doi_str_mv 10.1136/bjo.70.10.782
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subjects Biological and medical sciences
Child
Child, Preschool
Complex syndromes
Female
Humans
Laurence-Moon Syndrome - pathology
Male
Medical genetics
Medical sciences
Microscopy, Electron
Mitochondria - ultrastructure
Pedigree
Photoreceptor Cells - ultrastructure
Pigment Epithelium of Eye - ultrastructure
Retina - ultrastructure
Retinal Degeneration - genetics
Retinal Degeneration - pathology
title Histopathology of mitochondrial cytopathy and the Laurence-Moon-Biedl syndrome
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