Galactosemia is hereditary, but usually does not skip generations.

Hypophosphatemic rickets is primarily related to dietary and abnormal fetal growth and development. It does not have a generational inheritance, but it is necessary to strengthen physical examinations during the pregnancy of the second child, and special attention should be paid to nutrient intake after the child is born. If vitamin D2 is taken as vitamin D2, it must be taken orally or by intramuscular injection in large doses, or 1α-(OH)D3 or 1,25(OH)2D3 can be used.

The occurrence of cerebral palsy is associated with various factors, including infections during pregnancy, maternal diseases, newborn respiratory difficulties, and neonatal jaundice. Although some cases are caused by chromosomal abnormalities, which may carry a certain risk of hereditary transmission across generations, in most cases, it does not involve hereditary transmission across generations.

Phenylketonuria is a genetic disorder with an autosomal recessive inheritance pattern.

Understand the genetic possibilities and risks associated with pituitary dwarfism.

Although the risk of inheritance is low, if a mother develops vitiligo during breastfeeding, it is important to be cautious about the impact of treatment drugs on the child’s growth and development.

Retinal pigment disease is a genetic retinal degenerative disease, and there have been developments in genetic diagnosis and gene therapy.

Causes and Treatment Methods of Undescended Testicle Condition

Down Syndrome and Neural Tube Defects: Prenatal Screening and Diagnosis

Explore the current treatment status of Down syndrome, and understand how to help children with the condition through guidance and special training, as there is no cure available.