How does the third-generation IVF technique detect embryo chromosomal abnormalities

Neonatal genetic metabolic disease propionylcarnitine C3 abnormality requires follow-up examination and special dietary intervention

Phenylketonuria is a genetic disorder; what are its genetic conditions? How can it be prevented?

Understanding the Necessary Preparation and Projects for Pre-Marital Genetic Screening

This article introduces how to inquire about the causes of corpus callosum malformations and provides treatment and rehabilitation training recommendations for the condition.

Heterozygous mutations detected in infant hearing screening may simply indicate carrier status, and attention should be paid to changes in hearing. These mutations originate from genetics and may affect hearing. It is recommended to undergo regular hearing and language development checks.

The Probability of Genetic Transmission of Intellectual Disability and Testing Methods

Explore the different types of thalassemia and the interpretation of genetic testing results, providing professional medical insights.

Explore the definition, treatment methods, and the importance of genetic testing for HbH disease.

Discuss the natural and artificial induction of genetic mutations, and how to understand disease risks through genetic testing.