Intracerebral hemorrhage in a patient with glycogenosis type II (Pompe disease): Is there a pathophysiological relationship?

Muscle and Nerve

Volumn 38, Issue 3, 2008, Pages 1211-1212

  Brettschneider, Johannes ^a   Sperfeld, Anne D ^a   Ludolph, Albert C ^a   Kassubek, Jan ^a  

^a UNIVERSITY OF ULM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AGED; BRAIN HEMORRHAGE; CASE REPORT; DISEASE ASSOCIATION; FEMALE; GENE MUTATION; GLYCOGEN STORAGE DISEASE TYPE 2; HETEROZYGOTE; HUMAN; LETTER; ONSET AGE; PATHOGENESIS; PATHOPHYSIOLOGY; PRIORITY JOURNAL;

AGED; BRAIN; CEREBRAL HEMORRHAGE; FEMALE; GLYCOGEN STORAGE DISEASE TYPE II; HUMANS; MAGNETIC RESONANCE IMAGING;

EID: 51349098277     PISSN: 0148639X     EISSN: 10974598     Source Type: Journal    
DOI: 10.1002/mus.21076     Document Type: Letter

References (5)

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2. Fukuda T, Roberts A, Plot/ PH, Raben N. Acid alpha-glucosidase deficiency (Pompe disease). Curr Neurol Neurosci Rep 2007;7:71-77.
3. Hamilton BE. Cerebral amyloid disease. In: Osborn AG, editor. Diagnostic imaging: brain, 1st cd. Amirsys; 2004. p 58-62.
4. Kretzschmar HA, Wagner H, Hübner G, Danek A, Witt TN, Mehraein P. Aneurysms and vacuolar degeneration of cerebral arteries in late-onset acid maltase deficiency. J Neurol Sci 1990;98:169-183.
5. Makos MM, McComb RD, Hart MN, Bennett DR. Alpha-glucosidase deficiency and basilar artery aneurysm: report of a sibship. Ann Neurol 1987;22:629-633.