What BARTH SYNDROME means: Barth Syndrome - is a rare congenital metabolic and neuromuscular disorder that affects boys. It is passed from mother to son through the sex-linked, or X, chromosome. Symptoms affect multiple systems of the body and may include changes to metabolism, motor delays, hypotonia, delayed growth, cardiomyopathy, weakened immune system, chronic fatigue, lack of stamina, hypoglycemia, mouth ulcers, diarrhea, and varying degrees of physical and learning disability.
- Definition Behcet'S Disease:
- Dictionary Disease - is a chronic condition due to disturbances in the body's immune system. This system, which normally protects the body against infections through controlled inflammation, becomes over barth syndrome definition.
- Definition Batten Disease:
- Dictionary a rare, fatal, autosomal recessive neurodegenerative disorder that begins in childhood. Also known as Spielmeyer-Vogt-Sjogren-Batten disease, it is the most common form of a group of disorders barth syndrome explain.
- Definition Benign Intracranial Hypertension:
- Dictionary Hypertension - sometimes called benign intracranial hypertension (BIH) or pseudotumor cerebri (PTC) is a neurological disorder that is characterized by increased intracranial pressure (ICP), in the barth syndrome what is.
- Definition Bloch-Sulzberger Syndrome:
- Dictionary Syndrome - Incontinentia pigmenti (IP) is one of a group of gene-linked diseases known as neurocutaneous disorders. These disorders cause characteristic patterns of discolored skin and also involve barth syndrome meaning.
