Gray platelet syndrome.

The name GPS comes from the gray appearance of the platelets in the peripheral blood smear as a result of the absence of -granules. The genetic basis of GPS was recently demonstrated to be due to mutations in NBEAL2. The NBEAL2 gene encodes for the neurobeachin-like 2 (NBEAL2) protein, which is a member of the family of BEACH (BEige And Chediak-Higashi) domain-containing proteins on chromosome 3 (3p21). The NBEAL2 protein is likely involved in vesicular trafficking and may be critical for the development of -granules. Patients with GPS have a life-long predisposition to mucocutaneous bleeding and are also predisposed to develop myelofibrosis. This case illustrates the importance of inspection of the blood smear before making a diagnosis of ITP.