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What are common genetic disorders? Down syndrome (Trisomy 21). Fragile X syndrome. Klinefelter syndrome.
Summary Single-gene disorders, where a mutation affects one gene. Sickle cell anemia is an example. Chromosomal disorders, where chromosomes (or parts of chromosomes) are missing or changed. Chromosomes are the structures that hold our genes. Complex disorders, where there are mutations in two or more genes.
In this Page Heart disease. Asthma. Diabetes (sugar disease) Cancer. Single gene disorders.
The UNIQUE The Rare Chromosome Disorder Support Group is a non-profit, voluntary organization dedicated to promoting awareness of rare chromosomal abnormalities. The organization was founded in 1984 and served as a source of support and information for anyone affected by any rare chromosome abnormality.
Trisomy 13 (also called Patau syndrome) is a genetic disorder in which a person has 3 copies of genetic material from chromosome 13, instead of the usual 2 copies. Rarely, the extra material may be attached to another chromosome (translocation).

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Examples of genetic conditions include: some cancers. cystic fibrosis. high cholesterol. haemophilia. muscular dystrophy. birth defects (for example, spina bifida or a cleft lip).
Many genetic disorders result from gene changes that are present in essentially every cell in the body. As a result, these disorders often affect many body systems, and most cannot be cured. However, approaches may be available to treat or manage some of the associated signs and symptoms.
Skin cancer. Cardiomyopathies (hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmogenic cardiomyopathy and restrictive cardiomyopathy) arthritis. Inherited arrhythmia syndromes (sudden arrhythmic death syndrome, or SADS), long QT syndrome, Brugada, Catecholamainergic polymorphic ventricular tachycardia (CPTV

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