Progeria syndrome or Hutchinson-Gilford progeria syndrome (HGPS): Causes, treatment and prevention Definition

Progeria syndrome or Hutchinson-Gilford progeria syndrome (HGPS): Causes, treatment and prevention
Progeria is a rare genetic condition that causes a person to age prematurely. Children with progeria appear healthy, but by the age of 2 years, they look as if they have become old too fast.

In 1886, Hutchinson described the first patient with HGPS, a 6-year-old boy whose overall appearance was that of an old man. In 1887, Gilford described a second patient with similar clinical findings; in 1904, he published a series of photographs depicting the clinical manifestations of progeria at different ages. To date, approximately 100 patients with HGPS have been described in the literature.

The most common type of progeria syndrome is Hutchinson-Gilford progeria syndrome. It’s a rare and fatal genetic disorder. Wiedemann-Rautenstrauch syndrome is another type of progeria syndrome. It appears in children while they’re still in utero.

The adult version of progeria syndrome is Werner syndrome. The symptoms of Werner syndrome normally occur in teenagers. People with this condition may live into their 40s or 50s.

Genetic mutation: In 2003, researchers discovered that a mutation in the lamin A (LMNA) gene causes Hutchinson-Gilford progeria syndrome (HGPS). Normally, this gene provides the body with instructions on how to make proteins that hold the center of cells (called the nucleus) together. When this gene is mutated, one of these proteins, called lamin A, is not produced properly. As a result, the cells in the body are unstable and the nuclei become damaged over time. This makes the cells more likely to die prematurely and leads to symptoms of progeria. Cells in areas of the body that are frequently exposed to physical forces, either from inside or outside of the body (such as the cardiovascular and musculoskeletal systems), are particularly vulnerable to premature cell death.

Random occurrence: HGPS is not an inherited condition that is passed down from parents to their children. Instead, mutations in the LMNA gene randomly occur during the development of the sperm or egg. Therefore, people who have a child with progeria do not have an increased risk of having another child with the condition.

A newborn with progeria looks healthy, but by the age of between 10 months and 24 months, features of accelerated aging start to appear.

Signs of progeria include:

Limited growth and short stature
Lack of body fat and muscle
Loss of hair, including eyelashes and eyebrows
Early signs of skin aging, including thin skin
Stiffness in the joints
Visible veins
Narrow, wrinkled, or shrunken face
A head that is large compared with the body
A small jaw bone
Slow and abnormal tooth development
A high-pitched voice
Limited range of motion and possible hip dislocation
Generalized atherosclerosis, leading to cardiovascular and heart disease
Atherosclerosis (hardening of the arteries): Children with HGPS typically develop a condition called atherosclerosis, which occurs when the walls of the arteries become hard and thick.

Malnutrition: Malnutrition is another common complication of HGPS because some infants have difficulty feeding.

Osteoporosis: Patients with HGPS have an increased risk of developing progeria, a condition that causes the bones to become weak, brittle, and porous. As a result, children with progeria may have an increased risk of experiencing bone fractures than healthy children.

Diagnosis and tests
Since the symptoms are very noticeable, it’s likely that your child’s pediatrician will spot them during a routine checkup.
If you see changes in your child that seem like symptoms of progeria, make an appointment with your pediatrician or family doctor. Your doctor will do a physical exam, test hearing and vision, measure pulse and blood pressure, and compare your child’s height and weight to other kids the same age.
Afterward, if your pediatrician is concerned, you may need to see a specialist in medical genetics, who can confirm the diagnosis with a blood test.
Treatment and medications
There is no cure for progeria, but occupational and physical therapy can help the child keep moving if their joints are stiff.
Heart health is critical for people with progeria, so the doctor may prescribe statins, nitroglycerin for angina, and routine therapy for congestive heart failure.
Eating healthily and getting regular exercise are important.
Some patients may have cardiac surgery to slow the progression of heart disease.
Self-care tips may include eating different foods when the lipid, or fat, profile begins to change, and eating small meals regularly to maximize calorie intake.
Sun screen is important for protecting the skin, and padding in shoes can help minimize discomfort caused by a lack of fat padding on the body.
our child’s doctor may prescribe drugs to lower cholesterol or prevent blood clots. A low dose of aspirin every day can help prevent heart attacks and stroke. Growth hormone can help build height and weight.
At this time, there’s no cure for progeria, but researchers are working on finding one. A kind of cancer drug, FTIs (farnesyltransferase inhibitors), may fix the damaged cells.
There is no evident prevention for progeria since progeria is still a relative unknown and mysterious disease. However, it has been recently discovered that FTIs, a drug that has a possibility to help cure progiera, might also be abe to prevent the mishappen nuclei in progeria cells. After experiments, it showed that this drug was effective because it prevented the abnormal protein from reaching the scaffolding of the cell nucleus.


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