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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Research, diagnosis and education in inborn errors of metabolism in Colombia: 20 years’ experience from a reference center

Fig. 1

Diagnostic tests processed in the reference center. a Number of patient samples analyzed in the last 10 years. b Distribution of requested tests according to clinical suspicion in the last 10 years. AA: aminoacidopathies; OA: organic acidurias; LSD: lysosomal storage disorders; CD: carbohydrate disorders; PD: peroxisomal diseases (Total tests = 9772)

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