“…It is a critical coenzyme involved in DNA, proteins, lipid and carbohydrate metabolism. 8 Deficiency may arise due to intrinsic factor deficiency, achlorhydria, ileac disease, malnutrition, malabsorption syndromes, or a strict vegetarian diet. 9 The patients present with anemia, neurological manifestations such as loss of vibration, proprioception, spasticity, paraplegia, urinary incontinence, mucocutaneous features such as glossitis, angular cheilitis, localised or diffuse hair depigmentation and cutaneous hyperpigmentation of face, nails, acral pigmentation involving hands and feet, palmar creases and flexural surfaces.…”