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Adult gaucher disease in southern Tunisia: report of three cases

BACKGROUND: Gaucher disease (GD) is the most frequent lysosomal storage disorder; type 1 is by far the most common form. It is characterized by variability in age of onset, clinical signs and progression. It is usually diagnosed in the first or second decade of life with the appearance of bone pains...

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Bibliografiset tiedot
Päätekijät: Ben Rhouma, Faten, Kallel, Faten, Kefi, Rym, Cherif, Wafa, Nagara, Majdi, Azaiez, Hela, Jedidi, Ines, Elloumi, Moez, Abdelhak, Sonia, Mseddi, Sondes
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2012
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3275535/
https://ncbi.nlm.nih.gov/pubmed/22233685
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1746-1596-7-4
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