Neuropathy, hereditary sensory, type Id

Common Name(s)

Neuropathy, hereditary sensory, type Id

Autosomal dominant hereditary sensory neuropathy type 1D is characterized by adult onset of a distal axonal sensory neuropathy affecting all modalities, often associated with distal ulceration and amputation as well as hyporeflexia, although some patients may show features suggesting upper neuron involvement (summary by {1:Guelly et al., 2011}). For a discussion of genetic heterogeneity of HSAN, see HSAN1A ({162400}). Spastic paraplegia-3A (SPG3A; {182600}) is an allelic disorder with a different phenotype.
 

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Condition Specific Organizations

Following organizations serve the condition "Neuropathy, hereditary sensory, type Id" for support, advocacy or research.

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Scientific Literature

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