Syndrome

Sunset syndrome makes patients with neurological and degenerative diseases, such as Alzheimer’s disease, worse their symptoms in the late afternoon and evening, for no apparent reason. During this time, there are often more episodes of delirium, mental confusion and difficulty sleeping, especially if the person with the disease is an older person. At this time. […]

Parry-Romberg syndrome, or simply Romberg syndrome, is a rare disease characterized by skin atrophy, muscles, fat, bone tissue and facial nerves, resulting in aesthetic deformity; This disease usually affects only one side of the face, however, it can spread to the rest of the body. This disease is incurable, but medication and surgery help control

Clinical vampirism, also known as Renfield syndrome, is a psychological disorder associated with a blood obsession, a serious but rare disease, on which there are few scientific studies. People with this syndrome may experience various symptoms including an uncontrollable need to ingest blood, the desire to get hurt and cut off to suck their own

In rigid person syndrome, the individual has intense stiffness that can manifest throughout the body or only in the legs, for example, when they are affected the person can walk like a soldier because they cannot move their muscles and joints very well. It is an autoimmune disease that usually develops between the ages of

Mast cell activation syndrome is a rare disease that affects the immune system, resulting in allergic symptoms affecting more than one organic system, especially the skin and gastrointestinal, cardiovascular and respiratory systems, for example, the person may experience symptoms of skin allergy, such as redness and itching, as well as nausea and vomiting, for example.

Hanhart syndrome is a very rare disease characterized by the total or partial absence of the arms, legs or fingers, and this condition can occur at the same time on the tongue. The causes of Hanhart syndrome are genetic, although the factors that lead to these changes in the individual’s genes are not explained. Hanhart

Weaver syndrome is a rare genetic disease in which the child grows very fast throughout childhood, but has delays in intellectual development, as well as having characteristic facial features, such as a broad forehead and wide open eyes, for example. In some cases, some children may also have deformities in the joints and spine, as

Terson syndrome is an intraocular hemorrhage that occurs due to increased intracerebral pressure, usually as a result of a cranial hemorrhage due to a ruptured aneurysm or traumatic brain injury, for example. It is not known exactly how this bleeding occurs, which usually occurs in important areas of the eyes, such as vitreous, which is

Evans syndrome, also known as antiphospholipid syndrome, is a rare autoimmune disease, in which the body produces antibodies that destroy blood. Some patients with this disease may have only destroyed white blood cells or red blood cells alone, but the entire blood structure can be damaged in cases of Evans syndrome. The sooner the correct

Tetramelie syndrome is a very rare genetic disease that causes the baby to be born without arms or legs and can also cause other malformations of the skeleton, face, head, heart, lungs, nervous system, or genital area. This genetic alteration can still be diagnosed during pregnancy and therefore, depending on the severity of the malformations