Hello doctor! Doctor, can you tell me at what week of pregnancy can I determine XX or XY chromosomes? Thank you doctor.

Cerezyme (Imiglucerase) is used to treat certain rare genetic problems (such as Gaucher disease). Imiglucerase replaces a certain natural substance (an enzyme called glucocerebrosidase) that is missing in people with Gaucher disease. This medicine helps to improve blood, bone, liver and spleen problems caused by Gaucher disease. Imiglucerase does not correct the genetic problem and must be continued for life.

Crohn's disease is an inflammatory bowel disease with symptoms of abdominal pain, severe diarrhea, fatigue, weight loss, and malnutrition. The inflammation caused by Crohn's disease often spreads deep into the layers of intestinal tissue, which is both painful and debilitating, and can sometimes lead to life-threatening complications.

Cerebral palsy is a neuromuscular disorder that is often found in children. Therefore, many parents ask the question: Is cerebral palsy hereditary? Scientists believe that genetic disorders are one of the factors that cause the disease. However, is cerebral palsy really hereditary?

Thalassemia is a hereditary hemolytic anemia or congenital hemolytic anemia. The main symptom of the disease is anemia. Thalassemia causes serious complications and becomes a burden for families and society. However, the symptoms of the disease can be completely controlled with a reasonable thalassemia patient care regimen.

Thalassemia in children causes hemolytic anemia, which is considered a burden on the family and community, causing serious consequences for the race. Treating hemolytic anemia requires a lot of effort, time and compliance from the patient.

Thalassemia or hemolytic anemia is a disease that is passed from parents to children through a recessive genetic mechanism. A baby is born with the disease only if both the father and mother carry the disease gene. Currently, there are very simple hemolytic anemia tests that help determine the possibility of carrying the disease.

DNA fingerprints can be used to determine blood relationships, track down criminals through biological traces containing DNA left at the scene, or track down victims through living bodies, even if they are just bone fragments or teeth. This is a great advancement in forensic science.

Stickler syndrome is a group of genetic conditions characterized by distinctive facial features, eye abnormalities, hearing loss, and joint problems. A characteristic feature of Stickler syndrome is a somewhat flat face. This appearance is due to underdeveloped bones in the midface, including the cheekbones and bridge of the nose. A specific group of physical features called Pierre Robin syndrome is also common in people with Stickler syndrome. Problems with the bones of the spine can also occur, including abnormal curvature of the spine (scoliosis) and flattened vertebrae (spondylosis). Researchers have described several types of Stickler syndrome, distinguished by their genetic causes, signs, and symptoms. In this article, we will provide useful information to better understand Stickler syndrome.

Digestive malformations are common malformations in current medical literature. Most of these malformations need to be treated immediately, otherwise they will have consequences for the mother and baby. Early diagnosis of fetal malformations is extremely important for timely treatment. The following article provides us with knowledge about fetal gastrointestinal malformations.

Music is an art form that uses sound to express the emotions of the singer or listener. Its main elements are pitch (melodic adjustment), rhythm and tone. It is a combination of vocal sounds or sound instruments (or both) to create beauty of form, harmony and emotional expression. Therefore, it has many benefits for our health.