For infants with congenital glaucoma, early diagnosis and surgical treatment can control most cases and prevent further vision damage. However, due to their young age, babies may not be able to express symptoms, so parents should be vigilant and seek medical attention early. Long-term follow-up is required after surgery, and timely treatment for potential amblyopia should be provided.
Discusses the treatment of genetic metabolic disorders and potential complications.
Cri du Chat syndrome is a rare chromosomal short arm abnormality, occurring in one in every hundred thousand individuals. Its most distinctive feature is a crying sound resembling that of a cat.
Is Factor VIII deficiency a genetic disease? Can medication be used? Do you need surgery? What are some good methods?
Even without a family history of genetics, the risk of Down syndrome screening is indeed high, at 1/50, with a cutoff at 1/250, so amniocentesis is necessary.
What are the solutions to genetic problems related to malnutrition?
Expounds on the symptoms, diagnosis, and treatment methods of neurogenetic disorders.
Understanding the diagnostic process and precautions for pediatric neurological genetic diseases
Inquiry into Shanghai Jiuzhou Hospital’s treatment methods for Duchenne Muscular Dystrophy
Thalassemia is a common genetic disease, this article discusses the clinical symptoms and treatment methods of mild anemia.
