Baroreflex Syndrome
Baroreflex syndrome—often called afferent baroreflex failure—is a rare problem in the body’s blood-pressure “autopilot.” Normally, stretch sensors in the carotid arteries and aorta send signals to...
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Baroreflex syndrome—often called afferent baroreflex failure—is a rare problem in the body’s blood-pressure “autopilot.” Normally, stretch sensors in the carotid arteries and aorta send signals to...
Baroreflex failure is a disorder of the body’s automatic blood-pressure control system. In healthy people, pressure sensors (baroreceptors) in the carotid arteries and aorta send quick...
Axial spondylometaphyseal dysplasia is a very rare genetic bone growth disorder. “Axial” means the center line of the body (spine, ribs, pelvis, and nearby bones). “Spondylo-”...
Axial osteosclerosis means the bones of the axial skeleton become extra dense and hard. The axial skeleton is the spine, ribs, sternum, and pelvis. In axial...
Axial osteomalacia is an exceptionally rare bone disorder where the axial skeleton (spine, ribs, pelvis) develops a dense, coarse, sponge-like trabecular pattern on X-ray, but the...
Axial Mesodermal Dysplasia Spectrum (AMDS) is a rare condition that begins very early in pregnancy when the embryo is forming. It describes patients who show features...
Axenfeld-Rieger syndrome (ARS) is a rare genetic condition that mainly affects the front part of the eye (the “anterior segment”). It changes the way the iris,...
Axenfeld anomaly is a birth-time (congenital) change in the front part of the eye. The clear window of the eye (cornea) has a rim inside it...
Autosomal Recessive Spinocerebellar Ataxia 7 (SCAR7) is a very rare, inherited brain disorder that mainly affects the cerebellum (the balance and coordination center of the brain)....
SNX14 autosomal recessive cerebellar ataxia—often called SCAR20—is a rare, inherited brain disorder that starts in infancy or early childhood. Children have poor balance and coordination (ataxia),...
Autosomal Recessive Cerebellar Ataxia Caused by Mutation in SNX14 (SCAR20) is a rare, inherited brain disorder that starts in infancy or early childhood. Children develop problems...
Autosomal Recessive Spinocerebellar Ataxia 20 (SCAR20) is a very rare, inherited brain disorder that starts in infancy or early childhood. Children have trouble with balance and...