Porphyria, congenital erythropoietic

*Gene map locus 10q25.2-q26.3

CEP

Gunther disease

Porphyria, erythropoietic

UROS deficiency

Uroporphyrinogen III synthase deficiency

[Clinical features: mutilating photosensitivity; hemolytic anemia with splenomegaly]

[Inheritance: autosomal recessive]

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Congenital Erythropoietic Porphyria Successfully Treated by Allogeneic Bone Marrow Transplantation	Need for measurement of porphyrins in teardrops in patients with congenital erythropoietic porphyria	Ocular involvement caused by the accumulation of porphyrins in a patient with congenital erythropoietic porphyria
Blood	British Journal of Ophthalmology	British Journal of Ophthalmology


Ocular involvement in congenital erythropoietic porphyria (Gunther's disease): cytopathological evaluation of conjunctival and corneal changes	Ocular involvement in congenital erythropoietic porphyria (Gunther's disease): cytopathological evaluation of conjunctival and corneal changes	Congenital erythropoietic porphyria in two siblings
British Journal of Ophthalmology	British Journal of Ophthalmology	Dermatology Online Journal


Congenital erythropoietic porphyria in two siblings	Congenital erythropoietic porphyria in two siblings	Congenital erythropoietic porphyria in two siblings
Dermatology Online Journal	Dermatology Online Journal	Dermatology Online Journal


Congenital erythropoietic porphyria in two siblings	Congenital erythropoietic porphyria in two siblings	Congenital Erythropoietic Porphyria
Dermatology Online Journal	Dermatology Online Journal	DermIS


Congenital Erythropoietic Porphyria	Congenital Erythropoietic Porphyria	Congenital erythropoietic porphyria in three siblings
DermIS	DermIS	Indian Journal of Dermatology, Venereology and Leprology

23 images [ from 1 to 15 ]	1 2 next

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