Syndrome

Accelerated Thinking Syndrome is an alteration described by Augusto Cury, in which the mind is full of thoughts over the time the person is absent, hindering concentration, increasing anxiety and wearing down physical and mental health. Thus, the problem of this syndrome is not related to the content of thoughts, which are generally interesting, cultivated […]

PFAPA syndrome is a rare genetic disorder that develops in childhood up to age five. In this syndrome, your child develops monthly symptoms such as fever, foot-and-mouth disease, or pharyngitis and adenitis. This disease is mild and children with fever experience periods of fever lasting three to five days to 28 days apart. Between periods

A rare neurological disease is Sturge-Weber syndrome in which the individual has had seizures since birth, the syndrome also involves congenital glaucoma and the child has reddish spots on the face at birth, due to poor local vascularity, these spots usually affect only one side of the body and rarely the neck and trunk can

Lesch-Nyhan syndrome is an inherited disease, mainly affecting men, causing mental retardation, aggressive behavior, self-mutilation such as biting their fingers and lips and increasing uric acid production, leading to complications such as kidney stones and gouty arthritis. At birth, children with lesch-nyhan syndrome are apparently normal, but in the first few months of life they

Carpenter syndrome is a rare genetic disease, which is part of the acrocephalopolisindactyly disorder group. People with this syndrome are recognized by flattened skull, particular face, shortening of the fingers and toes, which are usually glued together, malformations of the forearms, extra fingers, mental retardation and motor difficulties. Symptoms are present from birth and development,

Bloom syndrome is a rare genetic disease characterized by a failure in the number of chromosomes, caused by a mutation of genes. People with Bloom syndrome have photosensitivity and deficiencies in their immune system, increasing the likelihood of developing diseases such as cancer and pneumonia, their symptoms appearing in the first few months of life.

Swyer syndrome, or purely gonadal dysgenia, is a rare disease in which a woman has male chromosomes and that is why her sex glands do not develop and does not have a very feminine image, her treatment is done with the use of synthetic female hormones for life, but it is not possible to get

Myoneural stress syndrome or myositis stress syndrome is a disease that causes chronic pain due to muscle tension caused by suppression of emotional and psychological stress. In mioneural stress syndrome, unconscious emotional problems such as anger, fear, resentment, or anxiety create tension in the autonomous nervous system that inhibits blood flow to muscles, nerves, and

Fanconi syndrome is a rare kidney disease that causes a buildup of glucose, bicarbonate, potassium, phosphates and certain excess amino acids in the urine. In this disease there is also a loss of protein in the urine and the urine becomes stronger and more acidic. Hereditary Fanconi syndrome causes genetic changes that are passed down