Wednesday, Nov 19, 2008 | 03:15 PM
MF_Images_6.jpg

Madisons Foundation - Moms And Dads In Search Of Needed Support

m-Power® Rare Pediatric Disease Database
Full disease list by letter:
3 | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | R | S | T | U | V | W | X | Y | Z | All

Results Page:   1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | Next

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. ...

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. ...

Albinism

Oculocutaneous Albinism, Ocular Albinism
Albinism is a group of disorders in which melanocytes, or pigment cells, are dysfunctional, causing a lack of pigmentation of the skin, eyes, and hair. Individuals are born with white hair and skin and the iris of the eye is translucent. In many cases, the skin, hair, and eyes will darken with age or with sun exposure. Additionally, individuals may have reduced vision. There are generally two ...
Results Page:   1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | Next

Full disease list by letter:
3 | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | R | S | T | U | V | W | X | Y | Z | All