Association of xeroderma pigmentosum with thrombasthenia

Hasanoglu A., Gucuyener K., Tumer L., Gursel T.

TURKISH JOURNAL OF PEDIATRICS, cilt.38, sa.2, ss.261-264, 1996 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 38 Sayı: 2
  • Basım Tarihi: 1996
  • Dergi Adı: TURKISH JOURNAL OF PEDIATRICS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.261-264
  • Gazi Üniversitesi Adresli: Hayır

Özet

Xeroderma pigmentosum (XP) is an autosomal recessive disorder characterized by severe sun-sensitivity, early skin cancers and abnormal DNA repair. XP has a worldwide distribution with an approximate frequency of 1/250,000. It Is classified into nine complementation groups, and distribution of patients among the various groups is related to ethnic origin.