August
12
20:06
Genetic Diseases

Ichthyosis Treatment

ichthyosis treatment Ichthyosis (crocodile skin, fish scales) - a rather rare, manifests in early childhood and runs a chronic hereditary anomaly of skin keratinization Causes Causesthat contribute to this disease is still not...
August
12
20:06
Genetic Diseases

Marfan syndrome

Marfan syndrome Marfan syndrome - a hereditary connective tissue diseases characterized by pathological changes in the nervous system, cardio - vascular system, musculo - skeletal system and other systems and organs of the human body. ...
August
12
20:06
Genetic Diseases

Phenylketonuria

Phenylketonuria Phenylketonuria (Felling disease) - a serious hereditary disease caused by metabolic disorders of amino acids and is manifested by progressive dementia, delay of physical development, disorders of muscle tone and moveme...
August
12
20:06
Genetic Diseases

Hailey - Hailey disease

Hailey - Hailey disease Hailey-Hailey (aka benign familial pemphigus) - a rare genetic dermatosis.Clinical manifestations of the disease - the flat flabby bubbles formed by erosion at the opening Manifestations Most often this ...
August
12
20:06
Genetic Diseases

Edwards Syndrome

Syndrome Edwards Edwards syndrome (trisomy of chromosome 18 pair) - the second most common chromosomal disorder after Down's syndrome, which is characterized by numerous defects fetal development, as well as underdevelopment of many sy...
August
12
20:06
Genetic Diseases

Colorblindness

blindness blindness - impaired ability to perceive certain colors having a hereditary nature, or caused by diseases of the retina or optic nerve.Retinal nerve cells called layer having an ability to transmit and receive light further i...
August
12
20:06
Genetic Diseases

Darier's disease

Darier disease Darier's disease (psorospermoz, follicular dyskeratosis, vegetating keratosis) - a chronic genetic disease of the skin, which is characterized by the appearance of the cone-shaped brownish or yellowish-brown nodules spec...
August
12
20:06
Genetic Diseases

Klinefelter's syndrome

Klinefelter's syndrome Klinefelter's syndrome - often occurring inherited genetic disorder caused by a change in the number of chromosomes.The disease is found only in males and is most clearly begins to emerge during puberty in the fo...
August
12
20:06
Genetic Diseases

The test for color blindness online

test for color blindness online Color blindness or color blindness - in most cases much less common hereditary or acquired feature of human vision, which is reflected in the inability to distinguish between multiple or single color.One...
August
12
20:06
Genetic Diseases

Apert Syndrome

Apert syndrome Apert's syndrome - a rare genetic disorder that is characterized by syndactyly, deformation of the front part of the skull and other defects on the part of the skeletal system.The first detailed description of the syndro...
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