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Evaluation and treatment of the newborn with epidermolysis bullosa.
Gonzalez ME. Gonzalez ME. Semin Perinatol. 2013 Feb;37(1):32-9. doi: 10.1053/j.semperi.2012.11.004. Semin Perinatol. 2013. PMID: 23419761 Review.
Epidermolysis bullosa (EB) is a heterogeneous group of inherited skin diseases characterized by increased skin fragility and variable degrees of extracutaneous involvement. The clinical spectrum ranges from localized skin disease to a life-threatening
Epidermolysis bullosa (EB) is a heterogeneous group of inherited skin diseases characterized by increased skin fragility and v
Autosomal recessive epidermolysis bullosa simplex. Generalized phenotypic features suggestive of junctional or dystrophic epidermolysis bullosa, and association with neuromuscular diseases.
Fine JD, Stenn J, Johnson L, Wright T, Bock HG, Horiguchi Y. Fine JD, et al. Arch Dermatol. 1989 Jul;125(7):931-8. doi: 10.1001/archderm.125.7.931. Arch Dermatol. 1989. PMID: 2662909 Review.
With few exceptions, epidermolysis bullosa (EB) simplex is an autosomal dominant disorder characterized by rather localized and recurrent nonscarring blister formation; mucous membranes and other organs are usually uninvolved. ...Our findings suggest that aut …
With few exceptions, epidermolysis bullosa (EB) simplex is an autosomal dominant disorder characterized by rather local …