Case study of Successful Treatment of Crigler Najjar syndrome by Homeopathy

How HomoeoCARE Treated a Newborn Infant with Crigler-Najjar Syndrome

A 1-month and 5-day-old yellow discolored infant was brought to HomoeoCARE with severe jaundice, persistent hypoglycemia, and hyperbilirubinemia. The infant was initially treated with phototherapy at birth but was later shifted to the NICU due to his symptoms and fluctuating bilirubin levels. The diagnosis was Crigler-Najjar Syndrome, an inherited disorder affecting the metabolism of bilirubin.

Crigler-Najjar Syndrome: An Overview

Crigler-Najjar Syndrome is a genetic disorder that affects the metabolism of bilirubin in the liver. Hemoglobin breaks down into heme and globin, which later decomposes into iron and biliverdin. The biliverdin then converts into bilirubin, which should be conjugated with glucuronic acid in the liver and excreted into bile and urine. When there is impaired liver uptake, impaired conjugation, or increased production of unconjugated bilirubin, it crosses the blood-brain barrier and causes damage to brain and nerve tissues.

Treating Crigler-Najjar Syndrome with HomoeoCARE

The infant was treated with homeopathic remedies at HomoeoCARE, and symptoms improved gradually. The infant's eyes and face started to look less yellow, indicating that the treatment was working. The treatment at HomoeoCARE was able to address the root cause of the disorder and support the infant's body in effectively metabolizing bilirubin.

These are the readings of his bilirubin