Create issue ticket

1,664 Possible Causes for Epidermolysis Bullosa

Show results in: Deutsch

  • Epidermolysis Bullosa Acquisita

    From Wikipedia, the free encyclopedia Jump to navigation Jump to search Epidermolysis bullosa acquisita Other names Acquired epidermolysis bullosa [1] Specialty Dermatology[] epidermolysis bullosa (disorder) EBA Epidermolysis bullosa acquisita EB acquisita Epidermolysis Bullosa Aquisita edit English epidermolysis bullosa acquisita chronic subepidermal[] In contrast to the genetic forms of epidermolysis bullosa, EBA is usually an acquired, sporadic disease.[]

  • Congenital Muscular Dystrophy

    Abstract Mutations in the PLEC1 gene encoding plectin have been reported in neonatal epidermolysis bullosa simplex with muscular dystrophy of later-onset (EBS-MD).[] Patients CMD with familial junctional epidermolysis bullosa often have brain atrophy and enlarged ventricles on MRI.[] Bullosa Simplex With Muscular Dystrophy Epidermolysis Bullosa Simplex And Limb-Girdle Muscular Dystrophy MD-EBS EBSMD MDEBS 226670 Genetic Test Registry Epidermolysis Bullosa[]

  • Esophageal Stenosis

    Epidermolysis bullosa (EB) is a disease with 3 forms, most hereditary, characterized by spontaneous blistering lesions.[] We report a 13-year-old boy with recessive dystrophic epidermolysis bullosa who had dysphagia due to esophageal stenosis.[] Dystrophic epidermolysis bullosa is caused by mutations in the COL7A1 gene encoding collagen VII, a protein of the epidermal attachment complex, and typically manifests with[]

  • Toxic Epidermal Necrolysis

    […] from his epidermolysis bullosa.[] Epidermolysis bullosa hereditaria. SLE. Scarlet fever (desquamation but no bullae). Other drug eruptions. Erythema multiforme. Bullous lichen planus.[] A 3-year-old child with recessive dystrophic epidermolysis bullosa treated with bone marrow transplantation subsequently developed body-wide epidermal detachment distinct[]

  • Epidermolysis Bullosa

    epidermolysis bullosa.[] Types Types of Epidermolysis Bullosa The different forms of epidermolysis bullosa include: Epidermolysis bullosa simplex —tissue separation and blistering occur in the top[] Who gets epidermolysis bullosa?[]

  • Dystrophic Epidermolysis Bullosa

    Epidermolysis bullosa nevi.[] Dystrophic epidermolysis bullosa (DEB) is one of the major forms of epidermolysis bullosa.[] bullosa acquisita.There exist other types of inherited epidermolysis bullosa, junctional epidermolysis bullosa and epidermolysis bullosa simplex, which are not related to[]

  • Junctional Epidermolysis Bullosa

    Epidermolysis bullosa Junctional epidermolysis bullosa (veterinary medicine) Skin lesion GeneReview/NIH/UW entry on Junctional Epidermolysis Bullosa[] Six types of junctional epidermolysis bullosa (JEB) have been described previously.[] bullosa (disorder) congenital junctional epidermolysis bullosa EBJ JEB Epidermolysis bullosa atrophicans Epidermolysis bullosa, junctional edit English junctional epidermolysis[]

  • Epidermolysis Bullosa Simplex

    Epidermolysis bullosa simplex is one of a group of genetic conditions called epidermolysis bullosa that cause the skin to be very fragile and to blister easily.[] epidermolysis bullosa simplex Also known as "Koebner variant of generalized epidermolysis bullosa simplex", presents at birth to early infancy with a predilection for the[] […] encoding keratin 5 or keratin 14 Epidermolysis bullosa simplex (disorder) Epidermolysis bullosa simplex Weber–Cockayne syndrome Statements Epidermolysis bullosa simplex Identifiers[]

  • Herlitz Disease

    What is Herlitz Junctional Epidermolysis Bullosa, LAMB3-related?[] Martin Carter Springer Science & Business Media , ٠٦‏/١٢‏/٢٠١٢ - 302 من الصفحات Because skin blisters are the initial manifestation of epidermolysis bullosa (EB), patients[] These findings supported a diagnosis of junctional epidermolysis bullosa. The patient was treated with topical and systemic antibiotics.[]

  • Mucous Membrane Pemphigoid

    No randomised controlled trials of treatments for epidermolysis bullosa acquisita were identified.[] These findings suggest that Brunsting-Perry cicatricial pemphigoid may represent a clinical variant of epidermolysis bullosa acquisita.[] Non-immune disorders that involve these epithelial components typically have a genetic basis--the main example being epidermolysis bullosa.[]

Further symptoms

Similar symptoms