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Amyotrophic cerebellar hypoplasia
Authors:G. A. de León  W. D. Grover  C. A. D'Cruz
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
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 ldquocerebellar hypoplasia in Werdnig-Hoffmann diseaserdquo, or ldquoanterior horn cell disease with pontocerebellar hypoplasiardquo. 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 ldquoamyotrophic cerebellar hypoplasiardquo (ACH) is a convenient designation for the syndrome.Supported in part by National Institutes of Health grant no. RR75
Keywords:Amyotrophy  Cerebellar hypoplasia  Malformation  Spinal muscular atrophy  Werdnig-Hoffmann disease
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