Congenital porphyria with necrotizing scleritis in a 9-year-old child

Clinical and Experimental Ophthalmology

Volumn 28, Issue 4, 2000, Pages 314-318

  Venkatesh, Pradeep ^a   Garg, S P ^a,b   Kumaran, Elan ^a   Tewari, Hem K ^a  

^a ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

^b Department of Ophthalmology ^*  (India)

Author keywords

[No Author keywords available]

Indexed keywords

ATROPINE; GLUCOMOL; PORPHYRIN; PREDNISOLONE; TIMOLOL MALEATE; UNCLASSIFIED DRUG;

ARTICLE; CASE REPORT; CHILD; CONGENITAL ERYTHROPOIETIC PORPHYRIA; FACE MALFORMATION; HUMAN; MALE; SCAR FORMATION; SCLERITIS; SKIN ALLERGY;

ATROPINE; CHILD; EYE PROTECTIVE DEVICES; HUMANS; MALE; NECROSIS; OPHTHALMIC SOLUTIONS; PORPHYRIA, ERYTHROPOIETIC; PREDNISOLONE; SCLERA; SCLERITIS; VISUAL ACUITY;

EID: 0033801494     PISSN: 14426404     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1442-9071.2000.00330.x     Document Type: Article

References (11)

1. The porphyrias
2. The porphyrias
3. Congenital porphyria. General and ocular manifestation
4. Ocular involvement in cutaneous porphyria, a clinical and histological report
5. Scleral involvement in symptomatic porphyria
6. Molecular analysis of uroporphyrinogen decarboxylase deficiency in a family with two cases of hepatoerythropoietic porphyria
7. Hepatoerythropoietic porphyria: Clinical, biochemical and enzymatic studies in a three generation family lineage
8. Ocular lesions in patients with porphyria
9. Escleromalacia observada en el curso de una porpirinuria cronica
10. Acute scleritis in porphyria cutanea tarda
11. Correction of congenital erythropoietic porphyria by bone marrow transfusion