What FARBER'S DISEASE - ALSO KNOWN AS FARBER'S LIPOGRANULOMATOSIS OR CERAMIDASE DEFICIENCY means: Farber's 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 and central nervous system. Most children with the disease die by age 2, usually from lung disease. In one of the most severe forms of the disease, an enlarged liver and spleen (hepatosplenomegaly) can be diagnosed soon after birth.
- Definition Fibromuscular Dysplasia - (FMD):
- Dictionary Dysplasia - (FMD) is an arterial disease of unknown etiology typically affecting the medium and large arteries of young to middle-aged women. In individuals with FMD, the walls of one or more farber's disease - also known as farber's lipogranulomatosis or ceramidase deficiency definition.
- Definition Fabry Disease:
- Dictionary caused by the lack of or faulty enzyme needed to metabolize lipids, fat-like substances that include oils, waxes, and fatty acids. The enzyme is known as ceramide trihexosidase, also called alpha farber's disease - also known as farber's lipogranulomatosis or ceramidase deficiency explain.
- Definition Familial Dysautonomia - FD, Sometimes Called Riley-Day Syndrome:
- Dictionary Dysautonomia - FD, sometimes called Riley-Day syndrome is a disorder of the autonomic nervous system which affects the development and survival of sensory, sympathetic and some parasympathetic farber's disease - also known as farber's lipogranulomatosis or ceramidase deficiency what is.
- Definition Febrile Seizures:
- Dictionary a convulsion in young children caused by a sudden spike in body temperature, often from an infection. During a febrile seizure, a child often loses consciousness and shakes, moving limbs on both farber's disease - also known as farber's lipogranulomatosis or ceramidase deficiency meaning.
