Understanding that hydrocephalus is not a genetic disease and the importance of early treatment for a child’s future development.

Cerebral palsy is a brain disorder caused by various different reasons, such as infections, skin breakdown, or injuries. Hereditary factors, including generational inheritance, could also be one of the causes.

Congenital epilepsy may be associated with genetics in some cases, but the extent of its influence depends on the cause. Most patients can marry and plan for children, but it is recommended to wait for at least six months after the condition is fully controlled and medication is stopped. Traditional Chinese medicine may offer unique benefits in treating epilepsy by regulating internal organs, potentially leading to a cure.

Inquired about his girlfriend’s mother having dwarfism, but his girlfriend’s height is normal, worried that their future child might also have dwarfism.

A seven-month-old baby has developed red rashes on the legs, with similar symptoms appearing on the arms a few days later. This could be psoriasis or eczema, and a doctor’s diagnosis is required. The family has a history of hereditary psoriasis, and the child feels itchy and exhibits scratching behaviors.

Explore the main symptoms of optic nerve atrophy, including vision degradation and changes in optic disc color, and introduce related examinations and treatments.

Discuss the genetic nature of the Hepatitis B virus and its prevention measures during pregnancy.

Patients with hypothyroidism can generally have normal fertility after their condition is stable and they receive appropriate treatment, but regular monitoring of thyroid function is required.

Discuss the treatment approaches for chronic colitis, address genetic questions, and explain the causes of mucous hemorrhage.

Explore the various possible causes of pediatric cerebral palsy, including genetic, infection, brain damage, and risk factors at different stages.