Amyotrophic cerebellar hypoplasia |
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Authors: | G. A. de León W. D. Grover C. A. D'Cruz |
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Affiliation: | (1) Department of Neurology, Temple University Hospital, 3401 North Broad Street, 19140 Philadelphia, PA, USA;(2) Dept. of Pathology, Temple University School of Medicine, 19140 Philadelphia, PA, USA;(3) Dept. of Pediatrics, Temple University School of Medicine, 19140 Philadelphia, PA, USA;(4) The St. Christopher's Hospital for Children, 19140 Philadelphia, PA, USA |
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Abstract: | Summary Lower motor neuron degeneration, cerebellar hypoplasia, atrophy of pons, olives, and cerebellum, sclerosis of thalamus and pallidum, and deficient myelination were found in a 2-months-old baby with laryngeal paralysis, mental retardation, progressive amyotrophy, and slow nerve conduction velocity. Such changes seem characteristic of an unusual syndrome previously referred to as cerebellar hypoplasia in Werdnig-Hoffmann disease, or anterior horn cell disease with pontocerebellar hypoplasia. Although the pathologic changes in lower motor neurons are indistinguishable from those in other cases of infantile spinal muscular atrophy, the consistent reproducibility of a complex pathologic pattern suggests that this is probably a manifestation of a separate disease process. The term amyotrophic cerebellar hypoplasia (ACH) is a convenient designation for the syndrome.Supported in part by National Institutes of Health grant no. RR75 |
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Keywords: | Amyotrophy Cerebellar hypoplasia Malformation Spinal muscular atrophy Werdnig-Hoffmann disease |
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