Literature DB >> 12084876

Clinicopathological features of genetically confirmed Danon disease.

K Sugie1, A Yamamoto, K Murayama, S J Oh, M Takahashi, M Mora, J E Riggs, J Colomer, C Iturriaga, A Meloni, C Lamperti, S Saitoh, E Byrne, S DiMauro, I Nonaka, M Hirano, I Nishino.   

Abstract

BACKGROUND: Danon disease is due to primary deficiency of lysosome-associated membrane protein-2.
OBJECTIVE: To define the clinicopathologic features of Danon disease.
METHODS: The features of 20 affected men and 18 affected women in 13 families with genetically confirmed Danon disease were reviewed.
RESULTS: All patients had cardiomyopathy, 18 of 20 male patients (90%) and 6 of 18 female patients (33%) had skeletal myopathy, and 14 of 20 male patients (70%) and one of 18 female patients (6%) had mental retardation. Men were affected before age 20 years whereas most affected women developed cardiomyopathy in adulthood. Muscle histology revealed basophilic vacuoles that contain acid phosphatase-positive material within membranes that lack lysosome-associated membrane protein-2. Heart transplantation is the most effective treatment for the otherwise lethal cardiomyopathy.
CONCLUSIONS: Danon disease is an X-linked dominant multisystem disorder affecting predominantly cardiac and skeletal muscles.

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Year:  2002        PMID: 12084876     DOI: 10.1212/wnl.58.12.1773

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  50 in total

1.  [Diagnosis and differential diagnosis of lysosomal glycogen storage disease].

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2.  LAMP-2 deficiency (Danon disease).

Authors:  S Di Mauro; K Tanji; M Hirano
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3.  Danon disease. A novel mutation in the LAMP-2 gene and ophthalmic abnormality.

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4.  Asymptomatic young man with Danon disease.

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5.  Hypertrophic Cardiomyopathy with Unusual Extensive Scarring Pattern: Danon Disease.

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Journal:  Methodist Debakey Cardiovasc J       Date:  2016 Oct-Dec

6.  Autophagy: Many paths to the same end.

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Review 7.  The utility of muscle biopsy.

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8.  Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey.

Authors:  P Charron; E Villard; P Sébillon; P Laforêt; T Maisonobe; L Duboscq-Bidot; N Romero; V Drouin-Garraud; T Frébourg; P Richard; B Eymard; M Komajda
Journal:  Heart       Date:  2004-08       Impact factor: 5.994

9.  Mosaic tissue distribution of the tandem duplication of LAMP2 exons 4 and 5 demonstrates the limits of Danon disease cellular and molecular diagnostics.

Authors:  Filip Majer; Ondrej Pelak; Tomas Kalina; Hana Vlaskova; Lenka Dvorakova; Tomas Honzik; Tomas Palecek; Petr Kuchynka; Martin Masek; Jiri Zeman; Milan Elleder; Jakub Sikora
Journal:  J Inherit Metab Dis       Date:  2013-05-29       Impact factor: 4.982

10.  Cardiovascular magnetic resonance findings in a case of Danon disease.

Authors:  Dorota Piotrowska-Kownacka; Lukasz Kownacki; Marek Kuch; Ewa Walczak; Agnieszka Kosieradzka; Anna Fidzianska; Leszek Krolicki
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