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Complex regional pain syndrome (CRPS type 1 and type 2), sometimes referred to by the hyponyms reflex sympathetic dystrophy (RSD) or reflex neurovascular dystrophy (RND), is a rare and severe form of neuroinflammatory and dysautonomic disorder causing chronic pain, neurovascular, and neuropathic symptoms.
This includes two separate types: type I and type II. Type I CRPS, formerly known as reflex sympathetic dystrophy (RSD) or "Sudeck's atrophy", refers to CRPS without any observed nerve damage. Type II, formerly known as causalgia, refers to CRPS with observed nerve damage. This form, similarly to other forms of AMPS, is known to be able to ...
Reflex Sympathetic Dystrophy Syndrome, the old name of the type I variation of the Complex regional pain syndrome. Reduced Swing Differential Signaling , an electronic signaling standard and protocol for a chip-to-chip interface.
Usual onset: 15–30 year old, typically ... Reflex sympathetic dystrophy; ... Patients with secondary Raynaud's can also have symptoms related to their underlying ...
Multisystem Inflammatory Syndrome in children MJD Machado-Joseph disease: ML mucolipidoses: MLD Metachromatic leukodystrophy: MMA Monomelic amyotrophy: MMR Measles, mumps, rubella: MMRV Measles, mumps, rubella, varicella: MND Motor neuron disease: MODY Maturity-onset diabetes of the young: MOH Medication overuse headaches: MPD ...
Reflex sympathetic dystrophy; see complex regional pain syndrome; Rejection sensitive dysphoria in psychology; RSD may also refer to: Science.
Reflex activation then results in systemic vasoconstriction below the spinal cord disruption. This peripheral arterial vasoconstriction and hypertension activates the baroreceptors . There is a resultant parasympathetic surge originating in the central nervous system which inhibits the sympathetic outflow.
Nearly all children with early onset or congenital muscular dystrophy type 1A (MDC1A) are unable to walk independently. Nevertheless, children with MDC1A are usually able to sit. Contrastingly, patients with late onset LAMA2-MD are usually able to walk independently. Of note, in both types of LAMA2-MD developmental motor milestones are delayed.