What CONGENITAL MYASTHENIA means: Congenital Myasthenia - is an inherited disorder that affects the transmission of signals to the muscles. It results from a variety of genetic defects at the molecules associated with neuromuscular transmission. Congenital myasthenia is not the same as myasthenia gravis, which is an autoimmune disorder. More than a dozen congenital myasthenic syndromes have been classified. Symptoms are usually noticed in early childhood and include drooping eyelids, facial weakness, and limb weakness. Parents of children with congenital myasthenia frequently show no symptoms of the disorder.
- Definition Central Pain Syndrome:
- Dictionary Syndrome - is a neurological condition caused by damage to or dysfunction of the central nervous system (CNS), which includes the brain, brainstem, and spinal cord. This syndrome can be caused by congenital myasthenia definition.
- Definition Ceramidase Deficiency:
- Dictionary Deficiency - Farber's disease describes a group of inherited metabolic disorders called lipid storage diseases, in which excess amounts of lipids (oils, fatty acids, and related compounds) build congenital myasthenia explain.
- Definition Coma And Persistent Vegetative State:
- Dictionary Vegetative State - A coma is a profound or deep state of unconsciousness. An individual in a state of coma is alive but unable to move or respond to his or her environment. Coma may occur as a congenital myasthenia what is.
- Definition Chorea:
- Dictionary abnormal voluntary movement disorder, one of a group of neurological disorders called dyskinesias, which are caused by over-activity of the neurotransmitter dopamine in the areas of the brain that congenital myasthenia meaning.
