Acid sphingomyelinase deficiency (Niemann-Pick disease types A and B)
Aug. 11, 2022
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Toll Free (U.S. + Canada): 800-452-2400
US Number: +1-619-640-4660
Support: service@medlink.com
Editor: editor@medlink.com
ISSN: 2831-9125
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Typical pedigree demonstrating the transmission of CADASIL through 5 generations. The index patient is indicated with an arrow. In this family, the disease demonstrates a typical autosomal dominant pattern of inheritance with roughly half of all at-risk individuals displaying the phenotype. (Contributed by Dr. Daniel Bonthius.)