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Ataxia describes lack of muscle coordination while performing voluntary movements. A sign of an underlying condition, ataxia can affect any part of your body.
Congenital adrenal hyperplasia is a genetic condition affecting the adrenal glands and interfering with normal growth and development in boys and girls.
Krabbe disease is a rare, inherited disorder — most often affecting infants — that impairs functioning of the central nervous system and usually leads to early death.
In myelofibrosis, healthy bone marrow is replaced with scar tissue, leading to severe anemia and fatigue.
Noonan syndrome is caused by a mutation in one of the genes responsible for normal development in many parts of the body, including the heart.
Polycythemia vera is a rare blood disorder in which a person's bone marrow makes too many blood cells.
Prader-Willi syndrome, a genetic disorder characterized by decreased muscle tone and a constant desire to eat, often leads to morbid obesity.
Stickler syndrome can affect multiple parts of your body, including your eyes, face, ears, bones and joints.
Thalassemia is an inherited blood disorder, characterized by less hemoglobin and fewer red blood cells than normal. When necessary, treatment includes blood transfusions.
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