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3 MONTH BABY SUFFERING FROM PRIMARY GENETIC HEMOPHAGOCYTIC LYMPHOTISTIOCYTOSIS

3 MONTH BABY SUFFERING FROM PRIMARY GENETIC HEMOPHAGOCYTIC LYMPHOTISTIOCYTOSIS

Master vijan hospital at KMCH COIMBATORE
  1. BABY VIJAN KMCH REG NO: 1683792, 3 MONTH AND 28 DAYS OLD BABY IS DIAGNOSED AS A CASE OF PRIMARY (GENETIC) HEMOPHAGOCYTIC LYMPHOTISTIOCYTOSIS A LIFE OF THEREATNING HISTOCYCTIC DIS ORDER TO AN UGC 13D GENETIC MUTATION . THE CURATIVE TREATMENT IS ALLOGENENIC TRANSPLANTATION , PREFERABLY HLA MATCHED SIBLING DONOR IS NOT AVAILABLE.
DETAILS OF THE CONCERN BABY

TOATAL COST OF THE TREATMENT WAS 21 LAKHS FOR THE BABY