Genetic Diseases

Muscular dystrophy is a chronic disease of the skeletal musculature of the human body, which ...

Syndrome Turner - a disease of genetic hereditary character, which results in disturbances in...

Hypochromic anemia is one of the common names for all forms of anemia that are characterized ...

Dwarfism( nanism, nanosomy, microsomy) is a clinical syndrome characterized by a delay in the...

Charcot's disease is a pathological process in which neurons of the central and peripheral CN...

Cretinism is a kind of one of the pathologies of the endocrine system, which is associated wi...

Cruson Syndrome is a rare genetic anomaly that has the second name of craniofacial dysostosis...

Albino is a person with a rare hereditary property, which is characterized by the absence of ...

Albinism in man manifests itself in the absence of normal pigmentation on the skin, hair, iri...