Gaucher disease with oculomotor apraxia and cardiovascular calcification (Gaucher type IIIC).
Neurology
; 54(1): 261-3, 2000 Jan 11.
Article
em En
| MEDLINE
| ID: mdl-10636167
ABSTRACT
The authors describe four siblings from consanguineous parents who presented with oculomotor deficit in early childhood characterized by impaired volitional horizontal saccades, compensatory lateral head thrust, and preservation of vertical movement. When about 10 years of age, heavily calcified aortic and mitral valves required surgery. Fibroblast beta-glucocerebrosidase activity was markedly reduced. Genotype analysis indicated that the two patients who were tested were homozygous for the D409H (1342G-->C) mutation. Relating this rare phenotype of Gaucher disease to D409H mutation will facilitate management of the disease and counseling of families.
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Base de dados:
MEDLINE
Assunto principal:
Apraxias
/
Calcinose
/
Doença de Gaucher
/
Doenças das Valvas Cardíacas
/
Músculos Oculomotores
Limite:
Adolescent
/
Female
/
Humans
/
Male
Idioma:
En
Ano de publicação:
2000
Tipo de documento:
Article