A case of aminolevulenic acid dehydratase deficiency porphyria (ALADP)

Springer Science and Business Media LLC - Tập 64 - Trang 433-434 - 1997
M. Nagaraj Rao1, J. Vijay Shekhar1, Vilayat Hussain1, Mohd Muneer1, Laxman1
1Department of Pediatrics and Biochemistry, P.D.S.C. Hospital, Hyderabad

Tài liệu tham khảo

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Plewinska, Met al. δ—Aminolevulinate dehydratase deficient prophyria: Identification of the molecular lesions in a severely affected homozygote.Am J Hum Genetics, 1991; 167: 49.

Desnick RJ, Anderson KE. Disorders of heme biosynthesis: The porphyrias. In: R. Hoffmanet al eds.,Hematology: Basic Principles and Practices, New York, Churchill Livingstone, 1991; 350–367.

Desnick RJ: The Porphyrias. In: Isselbacheret al eds,Harrisons Principles of Internal Medicine, KJ. New York, McGraw-Hill, 1994, 2073–2079.

Fujita Het al. Enzymatic defect in a child with hereditary hepatic porphyria due to homozygous δ—Aminolevulenic acid dehydratase deficiency: Immunochemical studies.Pediatrics, 1987; 880: 80.

Julian Chisolin J. Defects in heme pigment metabolism: The porphyrias. In: Richard E Behrmanet al eds,Nelson Textbook of Paediatrics, W.B. Saunders, 1992; 384–390.

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Springer Science and Business Media LLC

Tập 64

433-434

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