An autopsy case of G


Journal

Neuropathology : official journal of the Japanese Society of Neuropathology
ISSN: 1440-1789
Titre abrégé: Neuropathology
Pays: Australia
ID NLM: 9606526

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 06 02 2020
revised: 11 02 2020
accepted: 12 02 2020
pubmed: 29 3 2020
medline: 28 8 2021
entrez: 29 3 2020
Statut: ppublish

Résumé

G

Identifiants

pubmed: 32219895
doi: 10.1111/neup.12651
doi:

Substances chimiques

GLB1 protein, human EC 3.2.1.23
beta-Galactosidase EC 3.2.1.23

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

379-388

Informations de copyright

© 2020 Japanese Society of Neuropathology.

Références

Suzuki Y, Nanba E. β-Galactosidase deficiency (β-galactosidosis): GM1 gangliosidosis and Morquio B disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D, (eds). The Metabolic and Molecular Bases of Inherited Disease, 8th edn. New York: McGraw-Hill, 2001; 3775-3809.
Morrone A, Bardelli T, Donati MA et al. β-galactosidase gene mutations affecting the lysosomal enzyme and the elastin-binding protein in GM1-gangliosidosis patients with cardiac involvement. Hum Mutat 2000; 15: 354-366.
Caciotti A, Garman SC, Rivera-Colon Y et al. GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. Biochim Biophys Acta 1812; 2011: 782-790.
Suzuki K, Chen GC. Morphological, histochemical and biochemical studies on a case of systemic late infantile lipidosis (generalized gangliosidosis). J Neuropathol Exp Neurol 1968; 27: 15-38.
O'Brien JS, Ho MW, Veath ML et al. Juvenile GM1 gangliosidosis: Clinical, pathological, chemical and enzymatic studies. Clin Genet 1972; 3: 411-434.
Gilbert EF, Varakis J, Opitz JM et al. Generalized gangliosidosis type II (juvenile GM1 gangliosidosis). A pathological, histochemical and ultrastructural study. Z Kinderheilkd 1975; 120: 151-180.
Folkerth RD, Alroy J, Bhan I, Kaye EM. Infantile G(M1) gangliosidosis: Complete morphology and histochemistry of two autopsy cases, with particular reference to delayed central nervous system myelination. Pediatr Dev Pathol 2000; 3: 73-86.
van der Voorn JP, Kamphorst W, van der Knaap MS, Powers JM. The leukoencephalopathy of infantile GM1 gangliosidosis: Oligodendrocytic loss and axonal dysfunction. Acta Neuropathol 2004; 107: 539-545.
Kuki I, Tomiwa K, Okazaki S, Ikeda H, Kawawaki H. Late infantile GM1 gangliosidosis with progressive dilatation of common bile duct and obstructive apnea-an autopsy case (In Japanese with English abstract.). Brain Dev 2007; 39: 54-58.
Hachiya Y, Hayashi M. An 11-year-old boy showing rapid psychomotor regression and diffuse cerebral white matter lesions. Neuropathology 2009; 29: 517-519.
Nada R, Gupta K, Lal SB, Vasishta RK. An autopsy case of infantile GM1 gangliosidosis with adrenal calcification. Metab Brain Dis 2011; 26: 307-310.
Goldman JE, Katz D, Rapin I, Purpura DP, Suzuki K. Chronic GM1 gangliosidosis presenting as dystonia: I. Clinical and pathological features. Ann Neurol 1981; 9: 465-475.
Suzuki K. Neuropathology of late onset gangliosidoses. A review. Dev Neurosci 1991; 13: 205-210.
Yoshida K, Oshima A, Shimmoto M et al. Human beta-galactosidase gene mutations in GM1-gangliosidosis: A common mutation among Japanese adult/chronic cases. Am J Hum Genet 1991; 49: 435-442.
Richards S, Aziz N, Bale S et al. Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 2015; 17: 405-424.
Feng Y, Huang Y, Zhao X et al. Clinical and molecular characteristics of 11 Chinese probands with GM1 gangliosidosis. Metab Brain Dis 2018; 33: 2051-2057.
Yoshida K, Ikeda S, Kawaguchi K, Yanagisawa N. Adult GM1 gangliosidosis: Immunohistochemical and ultrastructural findings in an autopsy case. Neurology 1994; 44: 2376-2382.
Lee JS, Choi JM, Lee M et al. Diagnostic challenge for the rare lysosomal storage disease: Late infantile GM1 gangliosidosis. Brain Dev 2018; 40: 383-390.
Matsuda J, Suzuki O, Oshima A et al. Chemical chaperone therapy for brain pathology in G(M1)-gangliosidosis. Proc Natl Acad Sci U S A 2003; 100: 15912-15917.

Auteurs

Akiko Uchino (A)

Department of Neurology, Kitasato University Kitasato Institute Hospital, Tokyo, Japan.
Department of Neuropathology (Brain Bank for Aging Research), Tokyo Metropolitan Geriatric Hospital & Institute of Gerontology, Tokyo, Japan.

Makiko Nagai (M)

Department of Neurology, Kitasato University School of Medicine, Sagamihara-shi, Japan.

Naomi Kanazawa (N)

Department of Pathology, Kitasato University School of Medicine, Sagamihara-shi, Japan.

Masaaki Ichinoe (M)

Department of Pathology, Kitasato University School of Medicine, Sagamihara-shi, Japan.

Nobuyuki Yanagisawa (N)

Department of Pathology, Kitasato University School of Medicine, Sagamihara-shi, Japan.

Kaori Adachi (K)

Research Initiative Center, Tottori University, Tottori, Japan.

Eiji Nanba (E)

Research Strategy Division, Tottori University, Tottori, Japan.

Hiroyuki Ishiura (H)

Department of Neurology, The University of Tokyo, Tokyo, Japan.

Jun Mitsui (J)

Department of Molecular Neurology, The University of Tokyo, Tokyo, Japan.

Shoji Tsuji (S)

Department of Molecular Neurology, The University of Tokyo, Tokyo, Japan.
Institute of Medical Genomics, International University of Health and Welfare, Narita-shi, Japan.

Kinuko Suzuki (K)

Department of Neuropathology (Brain Bank for Aging Research), Tokyo Metropolitan Geriatric Hospital & Institute of Gerontology, Tokyo, Japan.

Shigeo Murayama (S)

Department of Neurology and Neuropathology (Brain Bank for Aging Research), Tokyo Metropolitan Geriatric Hospital & Institute of Gerontology, Tokyo, Japan.

Kazutoshi Nishiyama (K)

Department of Neurology, Kitasato University School of Medicine, Sagamihara-shi, Japan.

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