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Fig. 3. | Orphanet Journal of Rare Diseases

Fig. 3.

From: Failure to shorten the diagnostic delay in two ultra-orphan diseases (mucopolysaccharidosis types I and III): potential causes and implications

Fig. 3.

a Age at diagnosis in the RP and SP MPS III patients. b Time between the first visit to the GP for an MPS III-related symptom and the final diagnosis (in months) in the RP and SP MPS III patients. c Time between the first visit to a medical specialist for an MPS III-related symptom and the final diagnosis (in months) in the RP and SP MPS III patients. * p < 0.05; NS = non-significant

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