This review focuses on the description of three of the disorders, HSAN II through IV, that are characterized by autosomal recessive inheritance and onset at birth. These three forms of HSAN have been the most intensively studied, especially familial dysautonomia (Riley-Day syndrome or HSAN III...
Quantitative studies of dorsal root ganglia and neuropathologic observations on spinal cords in familial dysautonomia. J. Neurol. Sci. 35, 77–92 (1978). Article CAS PubMed Google Scholar Davidson, S. et al. Human sensory neurons: membrane properties and sensitization by inflammatory mediators....
(hypereosinophilic syndrome), severe renal failure, or inherited variations such as familial tryptasemia – a recently characterized disease which is associated with multisystem complaints including cutaneous flushing and pruritus, dysautonomia, functional gastrointestinal symptoms, chronic pain, and connective...
DYSAUTONOMIASLEEP disordersProdromal dementia with Lewy bodies (DLB) refers to a state prior to the onset of dementia with clinical signs or symptoms that may indicate the future development of DLB. Prodromal symptoms can include not only cognitive deficits but also a mix of clinica...