Chediak–Higashi syndrome (CHS) is an extremely rare autosomal recessive immunodeficiency
disorder characterized by partial oculocutaneous albinism, frequent pyogenic infections & presence of
abnormal large granules in leucocytes & other granule containing cells. Less than 500 cases have
been reported worldwide & only a few cases reports from India. Here, we report a case of CHS in a
one & half-year-old girl.
Page:
524-526
Download PDF:
