Isoleucine deficiency in a neonate treated for maple syrup urine disease masquerading as acrodermatitis enteropathica

Author:

Ross Benjamin,Kumar Manish,Srinivasan Hema,Ekbote Alka V.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference10 articles.

1. Gleason J. Avery’s Diseases of the Newborn. 9th ed. Philadelphia, PA: Saunders; 2011. p. 221–3.

2. Gene Reviews. Strauss KA, Puffenberger EG, Morton DH. Maple Syrup Urine Disease. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1319/. Accessed June 15, 2015.

3. Niiyama S, Koelker S, Degen I, Hoffmann GF, Happle R, Hoffmann R. Acrodermatitis acidemica secondary to malnutrition in glutaric aciduria type I. Eur J Dermatol. 2001;11: 244–6.

4. De Raeve L, De Meirleir L, Ramet J, Vandenplas Y, Gerlo E. Acrodermatitis enteropathica-like cutaneous lesions in organic aciduria. J Pediatr. 1994;124: 416–20.

5. Templier I, Reymond JL, Nguyen MA, Boujet C, Lantuejoul S, Beani JC, et al. Acrodermatitis enteropathica-like syndrome secondary to branched-chain amino acid deficiency during treatment of maple syrup urine disease. Ann Dermatol Venereol. 2006;133: 375–9.

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