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Wednesday, Dec 03, 2008 | 12:19 PM
Madisons Foundation - Moms And Dads In Search Of Needed Support
m-Power® Rare Pediatric Disease Database
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Agammaglobulinemia, X-linked (XLA)
Bruton's Agammaglobulinemia
X-linked agammaglobulinemia (XLA) is a disease of the immune system that presents in early childhood. There are many cells that work as part of the body’s immune system to help fight infection. One type of cell is the B lymphocyte which plays a part in producing a protein called immunoglobulins or antibodies. There are five major classes of immunoglobulins, and IgG (also called gamma globulin) is ...
Agenesis of the Corpus Callosum
Agenesis of the corpus callosum (ACC) is a rare anomaly of brain development that results in the partial or complete absence of a structure in the brain known as the corpus callosum. The corpus callosum is a group of fibers that serve as the bridge between the two sides of the brain. ACC is not a specific disease or syndrome itself, but rather is a description of a finding that can be seen in many...
Aicardi Syndrome
Aicardi syndrome is a very rare condition characterized by infantile spasms (a type of seizure condition), partial or complete absence of the corpus callosum (an area of brain nerve fibers connecting the right and left sides of the brain), and chorio-retinal lacunae (holes in the back of the eye). Only 300-500 cases have been described worldwide. It was first described by a French neurologist na...
Alagille Syndrome
Alagille syndrome (AGS) is a rare, genetically inherited disease. It is a disorder that affects many different organ systems, primarily the liver, heart, eyes, face, spinal skeleton and kidneys. The main problem people with AGS have is that they have fewer bile ducts in the liver than normal. The other features of AGS are highly variable from person to person.
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Alagille Syndrome (AGS)
What: Alagille syndrome (AGS) is a rare, genetically inherited disease. It is a disorder that affects many different organ systems, primarily the liver, heart, eyes, face, spinal skeleton and kidneys. The main problem people with AGS have is that they have fewer bile ducts in the liver than normal. The other features of AGS are highly variable from person to person.
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