Syndrome

Kallman syndrome is a rare genetic disease characterized by a delay in puberty and a reduction or absence of smell, due to a deficiency in the production of gonadotropin-releasing hormone. Treatment involves the administration of gonadotropins and sex hormones and should be done as soon as possible to avoid physical and psychological consequences. Symptoms depend […]

West syndrome is a rare disease characterized by frequent epileptic seizures, most common in children and beginning to appear during the baby’s first year of life; The first seizures usually occur between 3 and 5 months of life, although diagnosis can be made up to 12 months. There are 3 types of this syndrome, symptomatic,

Chest parade syndrome occurs when nerves or blood vessels between the collarbone and first rib are compressed, such as shoulder pain or tingling in your arms and hands. This syndrome is usually more common in women, especially those who have had a car accident or repeated chest injuries, but it can also develop in pregnant

Cushing syndrome is a disease caused by the high amount of cortisol in the blood, causing symptoms such as rapid weight gain and fat buildup in the abdominal and facial area, as well as the development of red veins in the body and fatty acne.prone skin like what. Diagnosis of this syndrome, also known as

Rotator cuff syndrome, also known as shoulder conflict syndrome, occurs when there is an injury to structures that help stabilize this area, causing symptoms such as shoulder pain, as well as difficulty or weakness in lifting the arm, and both may be due to tendinitis.partial or total rupture of tendons in the area. The rotator

Meniere syndrome is a rare disease that affects the inner ear, characterized by frequent episodes of dizziness, deafness and tinnitus, symptoms that usually appear suddenly and can last a few minutes or persist for hours, and the number and intensity of seizures varies from person to person. Although the exact causes of this syndrome are

Acute respiratory distress syndrome, also known as hialine membrane disease, respiratory distress syndrome, or only DRA, is a condition that occurs due to delayed development of the premature baby’s lungs, causing shortness of breath, rapid breathing, or wheezing. Normally, the baby is born with a substance called surfactant, which allows the lungs to fill with

Irritable bowel syndrome is a problem that causes inflammation of intestinal villlos, causing symptoms such as pain, bloating, excessive gas and periods of constipation or diarrhea; these symptoms are often aggravated by a variety of causes, ranging from stressful situations to eating certain foods. Thus, although this syndrome does not heal, it can be controlled

Down syndrome, or Down 21 syndrome, is a genetic disease caused by a chromosome 21 mutation that causes the carrier to have not a pair, but a trio of chromosomes, and therefore in total it does not have 46 chromosomes, but 47. This alteration of chromosome 21 causes the child to be born with specific

Zellweger syndrome is a rare genetic disease that causes alterations in the skeleton and face, as well as serious damage to important organs such as the heart, liver and kidneys, as well as lack of strength, hearing difficulties and seizures. Babies with this syndrome often show signs and symptoms within the first hours or days