Correction: Advanced strategies for detecting acid sphingomyelinase deficiency type B with attenuated phenotypes (Orphanet Journal of Rare Diseases, (2025), 20, 1, (252), 10.1186/s13023-025-03746-9)

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Abstract

Correction: Orphanet J Rare Dis 20, 252 (2025) Following publication of the original article [1], the authors reported an error in the numerical values of Fig. 1 in the published version. The incorrect version of Fig. 1 was: The Venn diagram illustrates the overlap between all types of conditions compatible with ASMD among selected patients with a cholesterol risk ratio > 4.5 n = 63 653). The numbers represent the cohort of patients derived from the total population. Individuals with a confirmed diagnosis of ASMD who met four or five diagnostic criteria are represented by grey points. Abbreviations: CT: Computed Tomography; GGOs: Ground-Glass Opacities The correct Fig. 1 is: The Venn diagram illustrates the overlap between all types of conditions compatible with ASMD among selected patients with a cholesterol risk ratio > 4.5 n = 63 653). The numbers represent the cohort of patients derived from the total population. Individuals with a confirmed diagnosis of ASMD who met four or five diagnostic criteria are represented by grey points. Abbreviations: CT: Computed Tomography; GGOs: Ground-Glass Opacities The original article [1] has been updated.

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Villeneuve, T., Jamme, T., Schwob, R., Levade, T., & Prévot, G. (2025, December 1). Correction: Advanced strategies for detecting acid sphingomyelinase deficiency type B with attenuated phenotypes (Orphanet Journal of Rare Diseases, (2025), 20, 1, (252), 10.1186/s13023-025-03746-9). Orphanet Journal of Rare Diseases . BioMed Central Ltd. https://doi.org/10.1186/s13023-025-03996-7

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