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- W2214883744 abstract "En Afrique, une maladie genetique telle que la maladie de Hurler est souvent de decouverte fortuite et a un stade avance. Le diagnostic evoque necessite une confirmation biologique et une prise en charge therapeutique difficiles. Observation Souleymane, âge de 10 ans, est hospitalise en mai 2001 pour dysmorphie faciale et regression des acquisitions [...]" @default.
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- W2214883744 date "2003-03-11" @default.
- W2214883744 modified "2023-09-23" @default.
- W2214883744 title "[Mucopolysaccharidosis Type 1 (Hurler's disease): the case of a ten-year-old boy]." @default.
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