ABO Neonatal Hemolytic Disease?

My daughter is about to turn one and has been diagnosed with ABO neonatal hemolytic disease, accompanied by intellectual and growth and development disabilities, enamel hypoplasia, and hearing impairment. I am asking for treatment methods to promote recovery.
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Accuracy of Newborn Disease Screening

Phenylketonuria is a genetic amino acid metabolism disorder, often inherited in an autosomal recessive manner across generations. When screening results are abnormal, early diagnosis and intervention should be carried out to avoid affecting the child’s growth, development, intelligence, and health. Parents should take their children to the doctor promptly and follow medical instructions for treatment.
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