CHARGE Syndrome

CHARGE syndrome is a complex genetic condition, which affects multiple systems in the body and sensory systems. It is the leading genetic cause of deafblindness worldwide, occurring in approximately 1 in 10,000 births. CHARGE syndrome is most often caused by...

Cystic Fibrosis

Other Names: Mucoviscidosis; CF Cystic fibrosis (CF) is a genetic disorder that causes mucus to build up and damage organs in the body, particularly the lungs and pancreas. Signs and symptoms may include salty-tasting skin; persistent coughing; frequent lung...

Cushing’s Syndrome

Other Names:  Cushing syndrome; Nodular primary adrenocortical dysplasia; Adrenal cortex adenoma; Hypercortisolism; Adrenal hyperfunction resulting from pituitary acth excess; Ectopic adrenocorticotropic hormone syndrome; Hyperadrenocorticism; Ectopic ACTH syndrome...

Sickle Cell Anemia

Other Names: HbS disease; Hemoglobin S Disease; Sickling disorder due to hemoglobin S. Sickle cell anemia is  is an inherited form of anemia — a condition in which there aren’t enough healthy red blood cells to carry adequate oxygen throughout your body,...
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