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Consensus clinical management guidelines for Acid Sphingomyelinase Deficiency (Niemann-Pick disease types A, B and A/B)
[post]
2022
unpublished
Background: Acid sphingomyelinase deficiency (ASMD) is a rare autosomal recessive disorder caused by mutations in SMPD1 gene. This rarity contributes to misdiagnosis, delayed diagnosis and barriers to good care. There is no published national or international guideline for diagnosis and management of patients with ASMD. For these reasons, we at INPDR have developed a clinical guideline that define standard of care for ASMD patients Methods: The information contained in these guidelines was
doi:10.21203/rs.3.rs-2206440/v1
fatcat:kqjiy34oq5gyjghprejfzcae44