August
12
20:06
Genetic Diseases

Crouzon syndrome

Crouzon syndrome Crouzon syndrome - a rare genetic anomaly that has the second name of craniofacial dysostosis and are characterized by different deformation front parts of the skull and brain.These deformations can be either congenita...
August
12
20:06
Genetic Diseases

Turner Syndrome

Syndrome Turner Turner syndrome - a genetic disease hereditary nature, which resulted in violations occur in the structure of the X chromosome, accompanied by abnormalities of the internal organs, and short stature.It is a hereditary d...
August
12
20:06
Genetic Diseases

Achondroplasia

Achondroplasia Achondroplasia - a genetic disease with infringement in the growth of bone tissue.This pathology is evident from birth.Besides achondroplasia it refers to the ancient birth defects and is characterized by disproportionat...
August
12
20:06
Genetic Diseases

Galactosemia

Galactosaemia Galactosemia - a disease with a rare disease that infants inherit from their parents.And they have a certain anomaly in an autosomal recessive gene, are its carriers.This vrozhdёnnost expressed malfunction in metabolism...
August
12
20:06
Genetic Diseases

Muscular dystrophy

Muscular Dystrophy muscular dystrophy - a chronic disease of the skeletal muscles of the human body, which has a hereditary character.In this disease marked muscle weakness and degeneration.Most individuals with this pathology is not a...
August
12
20:06
Genetic Diseases

Tuberous sclerosis

Tuberous sclerosis Tuberous sclerosis - a disease of genetic character fakomatoznoe that affects many organs and tissues, forming a benign tumor.To diagnose tuberous sclerosis is difficult due to the large number of marked clinical s...
August
12
20:06
Genetic Diseases

Angelman Syndrome

Angelman Syndrome Angelman Syndrome - a disease that refers to a genetic anomaly characterized by mental retardation and is accompanied by seizures, chaotic movements of hands, frequent laughter and smiles.The disease is also called ...
August
12
20:06
Genetic Diseases

Brittle bones

Osteogenesis imperfecta Osteogenesis imperfecta - congenital bone disease, as well as individual connective tissue structures.Another name osteogenesis imperfecta - brittle bone disease.The disease is inherited, that is,It is genetical...
August
12
20:06
Genetic Diseases

Wilson's disease

Wilson's disease Wilson's disease (Wilson's disease) - a disease that has a hereditary disease, which affects the liver and central nervous system as a result of violations of metabolic processes in the body of copper.Bezel yellow-brow...
August
12
20:06
Genetic Diseases

Cystic fibrosis

Cystic fibrosis Cystic fibrosis (from the Latin. «Muscus» - refers to the mucus or slimy, «viscidus» - sticky) - a heavy congenital disease characterized by lesions of exocrine glands and causes abnormal respiratory anddigestive system...
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