What FAMILIAL HEMANGIOMA - OR CAVERNOUS MALFORMATION means: Familial Hemangioma - or Cavernous malformation, is a rare disorder of the capillaries and smallest veins in one part of the brain. The disorder occurs when a blood-filled mass resembling a tumor, called a hemangioma, forms. Symptoms include headaches and seizures. Cavernous malformation is frequently inherited.
- Definition Fahr'S Syndrome:
- Dictionary Syndrome - also known as Idiopathic Basal Ganglia Calcification or Fahr's Syndrome is a rare, genetically dominant, inherited neurological disorder characterized by abnormal deposits of calcium familial hemangioma - or cavernous malformation definition.
- Definition Familial Idiopathic Basal Ganglia Calcification:
- Dictionary Familial Idiopathic Basal Ganglia Calcification - See Fahr's Syndrome above familial hemangioma - or cavernous malformation explain.
- Definition Familial Periodic Paralyzes:
- Dictionary Paralyzes - are a group of inherited neurological disorders caused by mutations in genes that regulate sodium and calcium channels in nerve cells. They are characterized by episodes in which the familial hemangioma - or cavernous malformation what is.
- Definition Farber'S Disease - Also Known As Farber'S Lipogranulomatosis Or Ceramidase Deficiency:
- Dictionary Disease - also known as Farber's lipogranulomatosis or ceramidase deficiency, describes a group of rare autosomal recessive disorders that cause an accumulation of lipids in the joints, tissues familial hemangioma - or cavernous malformation meaning.