CHEDIAK-HIGASHI SYNDROME

Dogan M., Acikgoz M., Bay A., Kaya A., Oner F.

NOBEL MEDICUS, cilt.5, sa.2, ss.65-67, 2009 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 5 Sayı: 2
  • Basım Tarihi: 2009
  • Doi Numarası: 10.1016/j.medcli.2009.11.021
  • Dergi Adı: NOBEL MEDICUS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.65-67
  • Van Yüzüncü Yıl Üniversitesi Adresli: Evet

Özet

Chediak-Higashi syndrome (CHS) is a rare autosomal recessive disorder of children and characterized by variable degrees of partial oculocutaneous albinism, increased susceptibility to recurrent pyogenic and respiratory tract infections with neutropaenia, impaired chemotaxis and bactericidal activity, and bleeding tendency as a result of deficient platelets.