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Sandhoff disease is a
lysosomal genetic,
lipid storage disorder caused by the
inherited deficiency to
create functional beta-hexosaminidases A and B. These...
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Hersha Parady (born
Betty Sandhoff; May 25, 1945 –
August 23, 2023) was an
American actress, best
known for her role of
Alice Garvey in
Little House on...
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better known by
their individual names: Tay–Sachs disease, AB variant, and
Sandhoff disease. Beta-hexosaminidase is a
vital hydrolytic enzyme,
found in the...
- Ruth
Sandhoff is a
German classically trained mezzo-soprano. Her
concert repertory ranges from
early Baroque to
contemporary music, with a
special fondness...
- neurons. Tay–Sachs
disease (along with AB-variant GM2-gangliosidosis and
Sandhoff disease)
occurs because a
mutation inherited from both
parents deactivates...
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syndrome Proteus syndrome Ritscher-Schinzel
syndrome Robinow syndrome Sandhoff disease Schneckenbecken dysplasia Sclerosteosis Severe X-linked myotubular...
- conditions,
classically Tay–Sachs disease, but also in Niemann–Pick disease,
Sandhoff disease, and mucolipidosis.
Metabolic Storage Diseases:, Tay–Sachs disease...
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Progressive supranuclear palsy Retinitis pigmentosa (RP)
Rheumatoid arthritis Sandhoff Disease Spinal muscular atrophy (SMA,
motor neuron disease)
Subacute sclerosing...
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therapy programs[which?] to
treat GM1
gangliosidosis and Tay–Sachs and
Sandhoff diseases. In June 2019,
Axovant announced a
strategic partnership with...
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disorders termed the GM2 gangliosidoses. Beta
subunit gene
mutations lead to
Sandhoff disease (GM2-gangliosidosis type II). The HEXB gene lies on the chromosome...