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Pseudo-Hurler polydystrophy
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#	Item
1	Pathways: Volume 6 No. 1 Summer 2004 A publication of ISMRD Add to Reading List Source URL: www.ismrd.org Language: English - Date: 2014-09-02 17:37:51 Medical genetics Lysosomal storage disease Glycoproteinosis Sialidosis Alpha-mannosidosis Fucosidosis Pseudo-Hurler polydystrophy Galactosialidosis I-cell disease Health Rare diseases Genetic genealogy
2	Pathways: March 2012: No. 2 A publication of ISMRD ISMRD wins $10,000 in Chase Community Add to Reading List Source URL: www.ismrd.org Language: English - Date: 2014-09-02 17:42:47 Lysosomal storage disease Medicine Pseudo-Hurler polydystrophy Sialidosis Mucolipidosis Fucosidosis I-cell disease Health Biology Glycoproteinosis
3	Pathways: Volume 8 No. 1 Summer \|Winter 2006 A publication of ISMRD Add to Reading List Source URL: www.ismrd.org Language: English - Date: 2014-09-02 17:45:03 Glycoproteinosis Alpha-mannosidosis Pseudo-Hurler polydystrophy Confide Sialidosis Fucosidosis Health Rare diseases Lysosomal storage disease
4	Pathways: 2009: No. 2 September 2009 A publication of ISMRD Add to Reading List Source URL: www.ismrd.org Language: English - Date: 2014-09-02 17:36:04 Lysosomal storage disease Rare disease Glycoproteinosis National Institutes of Health Pseudo-Hurler polydystrophy Sialidosis Disease Rare Disease Day Alpha-mannosidosis Health Medicine Epidemiology
5	What are Glycoprotein Storage Diseases? ? They are very rare, progressive and largely untreatable inherited genetic defects. Add to Reading List Source URL: www.ismrd.org Language: English - Date: 2014-09-02 17:45:22 Glycoproteinosis Lysosomal storage disease Alpha-mannosidosis Sialidosis Fucosidosis Pseudo-Hurler polydystrophy I-cell disease Mucolipidosis Aspartylglucosaminuria Health Rare diseases Biology