2006, Number 5
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Med Cutan Iber Lat Am 2006; 34 (5)
Junctional epidermolysis bullosa (Herlitz type)
Ruiz VR, Blasco MJ, Sánchez CD, Martínez LMJV
Language: Spanish
References: 5
Page: 237-238
PDF size: 154.82 Kb.
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REFERENCES
1.Nakano A, Chao SC, Pulkkinen L, Murrell D, Bruckner-Tuderman L, Pfendner E,Uitto J. Laminin 5 mutations in junctional epidermolysis bullosa: molecular basis of Herlitz vs non-Herlitz phenotypes. Hum Genet 2002;110(1):41-51.
Hauschild R, Wollina U, Bruckner-Tuderman L.Junctional epidermolysis bullosa gravis (Herlitz): diagnostic and genetic aspects. J Eur Acad Dermatol Venereol 2001;15(1): 73-6.
Basarab T, Dunnill MG, Eady RA, Russell-Jones R. Herlitz junctional epidermolysis bullosa: a case report and review of current diagnostic methods. Pediatr Dermatol 1997;14(4):307-11.
4.Marinkovich MP, Meneguzzi G, Burgeson RE, Blanchet-Bardon C, Holbrook KA, Smith LT, Christiano AM, Ortonne JP. Prenatal diagnosis of Herlitz junctional epidermolysis bullosa by amniocentesis. Prenat Diagn 1995;15(11): 1027-34.
5.Hausser I, Anton-Lamprecht I, Gustavii B. Prenatal diagnosis of junctional epidermolysis bullosa Herlitz type. Lancet 1989; 28;2(8670): 1035-6.
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