Moyamoya disease occurs in children and young adults and causes occlusion of the major cerebral vessels.5-8 Initial signs are usually strokes, seizures, ... AL Bernstein - 《Ajdc》 被引量: 21发表: 1993年 Moyamoya Disease Mimicking Encephalitis Moyamoya disease is a rare vaso-occlusive illness ...
SNH presenting in the 7th decade of life with status epilepticus is rare and we postulate that the cerebral atrophy associated with untreated HIV infection may have precipitated seizures in a predisposed individual. This case described demonstrates the importance including non-HIV related causes, when ...
Neonatal idiopathic primary hypoparathyroidism: A rare cause of neonatal seizures.HyperphosphatemiaHypocalcaemiaHypoparathyroidismNeonateSeizureEtiology of neonatal seizures (NNS) is diverse and hypocalcemia is one of the treatable causes. Neonatal hypocalcemia (NHC) due to congenital hypoparathyroidism, ...
Seizures frequently affect the heart rate and rhythm. In most cases, seizure-related cardiac changes are transient and do not appear to cause clinically significant abnormalities for the patient. Great interest in this area of research h... M Nei - 《Epilepsy Currents》 被引量: 93发表: 2009年...
Seizures Slurred speech Trouble swallowing Unsteady walk Vision problems Prion Disease Causes Prions are tiny proteins in your brain that don't act the way they should. They fold over the wrong way, spread, and then cause other proteins to form the same incorrect shape. ...
5). These disorders in general are not considered uncommon as a whole, but the collective group houses several rare monogenetic conditions; many of them being diagnosed at early childhood stages. Although cognitive and motor impairments are common to many of these conditions, seizures or epilepsy ...
Asystole Induced by Partial Seizures: : A Rare Cause of Syncope The clinical distinction between cardiovascular and epileptic causes of loss of consciousness is sometimes difficult, but becomes challenging when a primar... VALERIA,CARINCI,GAETANO,... - 《Pacing & Clinical Electrophysiology》 被引量...
Understanding these mechanisms is critical for developing treatments that address the underlying causes of diseases rather than merely the presenting symptoms. Moreover, the same dysfunctional series of interrelated symptoms implicated in rare recessive diseases may also lead to milder and potentially ...
The EveryLife Foundation for Rare Diseases commends the Food and Drug Administration (FDA) on today’s announcement of its intention to create a Rare Disease Innovation Hub. Co-chaired by CDER Director, Dr. Peter Marks, and CBER Director, Dr. Patrizia Cavazzoni,... « Older Entries ...
A large, international team of researchers led by scientists at the University of California, San Francisco has identified the gene that causes a rare childhood neurological disorder called PKD/IC, or "paroxysmal kinesigenic dyskinesia with infantile con