Microgastria

Microgastria: what is it and how does it affect health?

Microgastria is a rare congenital disease that is characterized by incomplete or partial atrophy of the stomach. The term microgastria comes from the Greek words micro (small) and gaster (stomach).

The stomach plays an important role in the digestion process, so disruption of its structure can lead to various health problems. Patients with microgastria may experience decreased appetite, nausea, vomiting, severe pain in the upper abdomen, nutritional deficiencies, and even delayed physical development.

Microgastria can be inherited genetically or occur as a result of certain anomalies in the development of the embryo. Diagnosis of this disease can be difficult because its symptoms can be similar to other gastrointestinal diseases. To make an accurate diagnosis, gastroscopy, x-ray or computed tomography may be required.

Treatment for microgastria depends on the severity of the disease and may include dietary adjustments, nutritional supplements, drug therapy, or even surgery. It is important to note that microgastria is an incurable disease, but with the right treatment, patients can improve their health and lifestyle.

In conclusion, microgastria is a rare disease that can have serious consequences for the patient's health. If you suspect you have this disease, consult your doctor for diagnosis. Early detection and treatment of microgastria can help maintain health and prevent complications from developing.

Microgastria is a rare hereditary disease that appears in early childhood and is characterized by the absence of the stomach or its reduction in size. This disease belongs to the group of malabsorption syndromes, that is, impaired absorption of nutrients in the gastrointestinal tract.

Microgastria appears in the first year of a child’s life. Boys are most often affected. The reasons for the development of this pathology are unknown. However, the role of hereditary factors has been established; for example, some children managed to inherit microgastria from their parents. In early childhood, in such children, parents and doctors often note rare stools with a foul odor; there may be mucus and blood in the stool.