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1,961 Possible Causes for Epidermolysis Bullosa, Syndactyly Does Not Occur, Total or Partial Syndactyly

  • Cenani Syndactylism

    On physical examination, bilateral ptosis, high and narrow palate, low-set ears, brachydactyly, and total partial syndactyly of the fingers, ulnar deviation of the fingers[] In some fetuses, this process does not occur completely between all fingers or toes and some residual webbing remains.[] bullosa with pyloric atresia EDAR ( EDAR Hypohidrotic ectodermal dysplasia ) · PTCH1 ( Nevoid basal cell carcinoma syndrome ) · BMPR1A ( BMPR1A Juvenile polyposis syndrome[]

  • 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.[]

    Missing: Total or Partial Syndactyly
  • Syndactyly

    Syndactyly A fusion of two or more toes or fingers. syndactyly partial/total webbing of some/all digits, due to soft-tissue and/or bone fusion across adjacent interdigital[] This condition does not have a notable cause and may occur in isolation or is inherited.[] Secondary syndactyly, also called "pseudosyndactyly", is rare and can be a complication of burns, dystrophic epidermolysis bullosa or trauma.[]

  • Intestinal Pseudo-Obstruction - Patent Ductus Arteriosus - Natal Teeth

    Postaxial polydactyly of the feet does occur, as does (partial) syndactyly of the second and third toes or third and fourth fingers.[] bullosa H00584 Epidermolysis bullosa simplex H00585 Epidermolysis bullosa, hemidesmosomal H00586 Epidermolysis bullosa, junctional [PATH: hsa04510 hsa04512 hsa04514 hsa04810[] Epidermolysis bullosa simplex: review and report of case. ASDC J Dent Child, 1998; 65(5):349-353. 70. Liu M, Huang W. Oral abnormalities in Taiwanese newborns.[]

    Missing: Total or Partial Syndactyly
  • 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.[] A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophy. J Clin Invest. 1996 Nov 15. 98(10):2196-200.[]

    Missing: Syndactyly Does Not Occur Total or Partial Syndactyly
  • 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.[] Recessive dystrophic epidermolysis bullosa (RDEB) is an inherited disorder of squamous epithelium that results in dystrophic scarring of the skin after minor trauma.[]

    Missing: Syndactyly Does Not Occur Total or Partial Syndactyly
  • Epidermolysis Bullosa Acquisita

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

    Missing: Syndactyly Does Not Occur Total or Partial Syndactyly
  • 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.[]

    Missing: Syndactyly Does Not Occur Total or Partial Syndactyly
  • Bullous Pemphigoid

    epidermolysis bullosa acquisita) or the epidermal side ('roof' for bullous pemphigoid) of the salt-split direct immunofluorescence specimen.[] bullosa.[] bullosa L12.31 Epidermolysis bullosa due to drug L12.35 Other acquired epidermolysis bullosa L12.8 Other pemphigoid L12.9 Pemphigoid, unspecified L13 Other bullous disorders[]

    Missing: Syndactyly Does Not Occur Total or Partial Syndactyly
  • 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[]

    Missing: Syndactyly Does Not Occur Total or Partial Syndactyly

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