The relationship between large Y chromosome and spontaneous abortion and abnormal embryo development

Does one spouse’s chromosomal abnormality lead to fetal stopping, and what is the complexity of this genetic trait?

Discussing the relationship between pediatric cerebral palsy and close kinship marriage

This condition is an autosomal recessive genetic disorder, characterized by the accumulation of phenylalanine and its ketones in the patient’s body, which are excreted in large amounts through urine. The main symptoms include intellectual disability, seizures, and reduced pigmentation.

Understanding the history of epilepsy in the family and the possibility of intergenerational inheritance is crucial for families planning to have children. This article will discuss the genetic mechanisms of epilepsy and how to assess and address potential genetic risks.

Understanding the importance of prenatal chromosomal screening and how to assess the risk of genetic diseases through the examination.

Chromosome 16 inversion may be related to the pathogenesis of leukemia, awaiting further research confirmation.

Discuss several types of chromosomal abnormalities and their impact on fertility and embryo development

Understanding the meaning of chromosomal abnormalities and strategies for resolving anal defecation difficulties

What medications should hypothyroid patients take for treatment, and how can the condition be controlled?