Clinical diagnosis of Fabry disease whorl-like corneal opacity

Neurology

Volumn 60, Issue 6, 2003, Pages 1048-

  Yoshikawa, Hideto ^a   Ogawa, Izumi ^b  

^a NIIGATA CITY GENERAL HOSPITAL   (Japan)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GALACTOSIDASE;

ARTICLE; BODY TEMPERATURE; CASE REPORT; CHILD; CONTROLLED STUDY; CORNEA OPACITY; ENZYME ACTIVITY; FABRY DISEASE; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HEART FUNCTION; HUMAN; HYPESTHESIA; KIDNEY FUNCTION; LABORATORY TEST; LEUKOCYTE; OCULAR PRURITUS; OPHTHALMOLOGY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SLIT LAMP; SWEATING;

EID: 0037465772     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000048563.17902.5E     Document Type: Article

References (2)

1. Lou HOC, Heidensleben E, Larsen HW. The value of ocular findings in the diagnosis of angiokeratoma corporis diffusum (Fabry's disease). Acta Opthalmol 1970;48:1185-1194.
2. Sher NA, Letson RD, Desnick RJ. The ocular manifestations in Fabry's disease. Arch Opthalmol 1979;97:671-676.