2017
DOI: 10.4103/ijpd.ijpd_16_17
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Inherited epidermolysis bullosa: A multisystem disease of skin and mucosae fragility

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Cited by 6 publications
(2 citation statements)
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“…Epidermolysis bullosa (EB) is a group of rare heritable diseases characterized by blistering and fragile skin. It is associated with anomalies such as palmar-plantar thickening, syndactyly, dysphagia, gingival hyperkeratosis, cardiomyopathy, and osteoporosis (Maldonado-Colin et al, 2017). The blistering results from mechanical stress that eventually gives rise to chronic wound conditions (Medeiros and Riet-Correa, 2015).…”
Section: Skin Diseasesmentioning
confidence: 99%
“…Epidermolysis bullosa (EB) is a group of rare heritable diseases characterized by blistering and fragile skin. It is associated with anomalies such as palmar-plantar thickening, syndactyly, dysphagia, gingival hyperkeratosis, cardiomyopathy, and osteoporosis (Maldonado-Colin et al, 2017). The blistering results from mechanical stress that eventually gives rise to chronic wound conditions (Medeiros and Riet-Correa, 2015).…”
Section: Skin Diseasesmentioning
confidence: 99%
“…Epidermolysis Bullosa (EB) is an inherited mechanobullous disorder with an incidence of 1: 50 000 live birth/year [ 1 ]. In this case report, we describe an uncommon presentation of epidermolysis bullosa simplex (EBS) in neonates born to a mother with Epidermolysis bullosa pruriginosa (EBP).…”
Section: Introductionmentioning
confidence: 99%