A new case of oculocerebral hypopigmentation syndrome (Cross syndrome) with additional findings


Tezcan I., Demir E., Asan E., Kale G., Muftuoglu S. , Kotiloglu E.

CLINICAL GENETICS, cilt.51, sa.2, ss.118-121, 1997 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 51 Konu: 2
  • Basım Tarihi: 1997
  • Dergi Adı: CLINICAL GENETICS
  • Sayfa Sayıları: ss.118-121

Özet

Cross syndrome is a rare syndrome characterized by ocular and cutaneous hypopigmentation and neurological manifestations. A few reports have been published since 1967. In this report, we present a new case of Cross syndrome with additional findings such as urinary tract abnormality, bilateral inguinal hernia, focal interventricular septal hypertrophy of the heart and vacuolization of myeloid series cells and distinct ultrastructural features of the skin.