NIMS Medical Genetics Department: A beacon of hope for rare disease patients

NIMS Medical Genetics Department: A beacon of hope for rare disease patients

The department treats a spectrum of rare conditions, including Gaucher Disease, Homocystinuria, Growth Hormone Deficiency, Methylmalonic Acidemia, Wilson Disease, Phenylketonuria, and Pompe Disease, among others The department treats a spectrum of rare conditions, including Gaucher Disease, Homocystinuria, Growth Hormone Deficiency, Methylmalonic Acidemia, Wilson Disease, Phenylketonuria, and Pompe Disease, among others Hyderabad Health News, Wellbeing Tips, Diseases, Treatment and Nutrition | The Hindu

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