HYDROCEPHALUS, CORNEAL OPACITIES, DEAFNESS, LEFT-VENTRICLE HYPERTROPHY, CLINODACTYLY IN AN ADOLESCENT PATIENT - A NEW SYNDROME-ASSOCIATED WITH GLUCOCEREBROSIDASE DEFICIENCY


ERDURAN E. , MOCAN H., GEDIK Y. , KAMACI R., OKTEN A. N. , DEGER O.

GENETIC COUNSELING, cilt.6, ss.211-215, 1995 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 6 Konu: 3
  • Basım Tarihi: 1995
  • Dergi Adı: GENETIC COUNSELING
  • Sayfa Sayıları: ss.211-215

Özet

Hydrocephalus, corneal opacities, deafness, left ventricle hypertrophy, clinodactyly in an adolescent patient. A new syndrome associated with glucocerebrosidase deficiency: We report a 12-year-old girl with an unusual phenotype of Gaucher disease type 3. Liver glucocerebrosidase activity was 20% of the normal. In addition to common manifestations such as hepatomegaly, she showed primary communicating hydrocephalus, corneal opacities, deafness, left ventricle hypertrophy, and clinodactyly of hands and feet. We suspect cardiomyopathy to be due to myocardic infiltration with Gaucher cells, and corneal opacities to result from an accumulation of lipid-like inclusions into the posterior stromal keratinocytes. We were only able to find one previously published sibship disclosing similar features, which could allow the delineation of a new clinical variant of Gaucher disease.