Chromosomal disorders are genetic conditions that require a thorough chromosome check during pre-pregnancy screening to prevent passing them on to the next generation.

Phenylketonuria is a common chromosomal recessive genetic disease with no cure available at present, requiring lifelong treatment.

Discussing whether vitiligo is hereditary and its impact on fertility.

Diabetes is not a genetic disease, but if there are diabetes patients in the family, the child’s risk of developing the disease is higher.

Pediatric white matter dysplasia may be caused by genetic factors, with varied symptoms and prognosis depending on the progression of the condition and treatment.

What are the characteristics of chromosomal disorders?

Pediatric paralysis is not a genetic disease but a condition caused by a postnatal infection.

G6PD deficiency, commonly known as sickle cell anemia, is a genetic disorder caused by a lack of glucose-6-phosphate dehydrogenase (G6PD) in red blood cells. This article discusses its genetic factors, other causes, and preventive and treatment methods.

If a child exhibits symptoms such as jaundice, loss of appetite, vomiting, and digestive problems with pale yellow or grayish stools, they should seek medical attention immediately to check for galactosemia and avoid self-administering unknown medications.

Is there a possibility of curing Type 1 diabetes in children, and where can one find authoritative hospitals for treatment?