Search results
Results From The WOW.Com Content Network
Myotonia congenita is a congenital neuromuscular channelopathy that affects skeletal muscles (muscles used for movement). It is a genetic disorder.The hallmark of the disease is the failure of initiated contraction to terminate, often referred to as delayed relaxation of the muscles and rigidity. [1]
Drowsiness, yawning, disinclination for work, lack of social participation, mood changes, apathy, sleep disturbances, other fatigue-related symptoms The sopite syndrome ( / s oʊ ˈ p aɪ t / ; from Latin sopire 'to put to sleep') [ 1 ] is a neurological disorder that relates symptoms of fatigue , drowsiness , and mood changes to prolonged ...
Research data strongly suggest that neither contagious nor story-induced yawning is reliable in children below the age of six years. [8] Nervousness, which often indicates the perception of an impending need for action, has also been suggested as a cause. Anecdotal evidence suggests that yawning helps increase a person's alertness.
Yawning. We all do it and yet there's no set explanation on why we do it. And just as mysterious is that the act of yawning seems to be contagious. A new study looking at that issue has found that ...
The Moro reflex may be observed in incomplete form in premature birth after the 25th week of gestation, and is usually present in complete form by week 30 (third trimester). [1] Absence or asymmetry of either abduction or adduction by 2 to 3 months age can be regarded as abnormal, as can persistence of the reflex in infants older than 6 months. [3]
Excessive yawning is usually no cause for concern and likely just indicates drowsiness. However, in some cases, extra yawns can flag something more serious, ...
Similarities to other conditions, as well as normal pregnancy features, commonly lead to misdiagnosed cases or more often, delayed diagnosis. [ 6 ] [ 25 ] There is a general consensus regarding the main three diagnostic criteria of HELLP syndrome, which include hepatic dysfunction , thrombocytopenia and microangiopathic haemolytic anaemia in ...
Spina bifida (SB; /ˌspaɪnə ˈbɪfɪdə/, [9] Latin for 'split spine') [10] is a birth defect in which there is incomplete closing of the spine and the membranes around the spinal cord during early development in pregnancy. [1]