Hypoplasia is a medical condition in which an organ or tissue does not develop properly during fetal development. It can affect any organ or tissue in the body, including the heart, lungs, kidneys, muscles, and bones.
What Causes Hypoplasia?
Hypoplasia can be caused by a variety of factors, including genetic mutations, infections, and exposure to toxins. It may also be caused by an inherited condition, such as Down syndrome.
What Are the Symptoms of Hypoplasia?
The symptoms of hypoplasia vary depending on what organ or tissue is affected. Some common symptoms include shortness of breath, chest pain, weakened muscles, and slow growth in children.
How Is Hypoplasia Diagnosed?
Hypoplasia is diagnosed with physical exams, imaging tests, and blood tests. A doctor may also order genetic tests to look for genetic mutations or inherited conditions.
How Is Hypoplasia Treated?
Treatment for hypoplasia depends on the severity of the condition and the affected organ or tissue. In some cases, treatment may include medications, surgery, or physical therapy. In other cases, the condition may not require any treatment.