May
11
23:01
Genetic Diseases

Polydactyly

Polydactyly Polydactyly - this anatomical anomaly, which is characterized by congenital change in the number of fingers on the foot or leg.This disease has a double origin.In the first case, the splitting of the fingers occurs along th...
May
10
23:01
Genetic Diseases

Dwarfism

Dwarfism Dwarfism (dwarfism, nanosomes, microsomia) - a clinical syndrome, which is characterized by delayed physical development of man (hence the name of the disease: dwarfism with Greek - "dwarf").There are proportionate dwarfism an...
May
10
23:01
Genetic Diseases

Homogentisuria

homogentisuria homogentisuria - it is a rare genetic disorder that develops as a result of an absolute deficiency of the enzyme homogentisic acid, shown in black urine output.This disease is characterized by disorder of tyrosine metabo...
May
09
23:01
Genetic Diseases

Albinism

Albinism Albinism in humans manifests itself in the absence of normal pigmentation of the skin, hair and iris.This anomaly is a hereditary trait, depending on the presence of recessive genes suppressed in the homozygous state.Albinism ...
May
09
23:00
Genetic Diseases

Arachnodactyly

arachnodactyly arachnodactyly - is one of the symptoms of Marfan syndrome.Arachnodactyly first described by the famous French pediatrician Marfan (Marfan), giving it the name dolichostenomelia, which is still called Marfan's disease. ...
May
08
23:01
Genetic Diseases

Tetra-Sachs syndrome

Syndrome Tetra Amelia syndrome, Tetra-Amelia - is a hereditary, congenital and very rare disease, which is characterized by the absence of the four limbs.Often, other body parts can also be exposed malformations.This refers to the skul...
May
08
23:01
Genetic Diseases

Hypochromic anemia

hypochromic anemia hypochromic anemia - is one of the common names for all forms of anemia, characterized by lack of hemoglobin, where the quantitative indicator of the color of blood is less than 0.8.Basically when hypochromic anemia ...
May
07
23:00
Genetic Diseases

Albino

Albino albino - a man with a rare hereditary property, which is characterized by a lack of pigmentation in the iris of the eye, skin, hair.This anomaly, speaking hereditary phenomenon, largely depends on the presence of overwhelming re...
May
07
23:00
Genetic Diseases

Aschistodactylia

syndactyly syndactyly - the development of vice, which is characterized by a seam between one or more fingers on the foot or hand to their functional impairment or lesions of certain cosmetic segment.Syndactyly occurs almost twice as o...
May
06
23:00
Genetic Diseases

Prader-Willi syndrome

Prader-Willi syndrome Prader-Willi syndrome - a genetic rare anomaly characterized by stop working genes, or in a scientific phenomenon caused by lack of expressing that means the transfer of genetic information from DNA to RNA.The fun...
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