Ocular involvement caused by the accumulation of porphyrins in a patient with congenital erythropoietic porphyria [7]

British Journal of Ophthalmology

Volumn 85, Issue 10, 2001, Pages 1265-1266

  Kurihara, K ^a   Takamura, N ^a   Imaizumi, S ^a   Yamashita, S ^a   Kondo, M ^a  

^a NAGASAKI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CONGENITAL ERYTHROPOIETIC PORPHYRIA; EYE DISEASE; GENE MUTATION; HUMAN; LACRIMAL FLUID; LETTER; MALE; PRIORITY JOURNAL; SCLERA DISEASE; VISUAL ACUITY;

ADULT; HUMANS; MALE; NECROSIS; PORPHYRIA, ERYTHROPOIETIC; SCLERA; SCLERAL DISEASES; TEARS;

EID: 0034816160     PISSN: 00071161     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (4)

1. Molecular aspects of the inherited porphyrias
2. Prenatal exclusion of congenital erythropoietic porphyria (Günther's disease) in a fetus at risk
3. Ocular complication in congenital erythropoietic porphyria
4. Congenital erythropoietic porphyria: Identification and expression of 10 mutations in the uroporphyrinogen III synthase gene