Madisons Foundation - Moms And Dads In Search Of Needed Support

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Coffin-Siris syndrome (CSS) is a rare, inherited, genetic condition that is characterized by mental retardation, specific facial features, and unique alterations in the fifth fingers and toes. Children have symptoms at birth and usually have affected family members. ...

Cogan syndrome is a rare disorder that causes dizziness, hearing problems and inflammation of the eyes. It can also sometimes affect blood vessels in other parts of the body. ...

Cohen syndrome is a genetic disorder that is characterized by low muscle tone of the body in infancy and obesity in childhood. Intelligence is also mildly to moderately affected in most children. ...

Common variable immunodeficiency (CVID) is an immunological disorder of antibody production. An antibody is a protein that attaches to an invading particle and leads to its destruction. The body makes several classes of antibodies, or immunoglobulins (Ig), including IgG, IgA, IgE, IgD, and IgM. People with CVID have low antibody levels (especially IgG, IgA, and IgM) and thus experience repeated in...

Complement deficiencies are a group of disorders characterized by the absence of a particular complement protein that functions in the immune system. The complement system is a system of proteins that work together and have many important responsibilities. It targets harmful bacteria so that they can be recognized, swallowed, and eliminated by white blood cells known as phagocytes. It punches hole...

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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