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1,972 Possible Causes for Epidermolysis Bullosa, Fused Ulna and Radius, Syndactyly Does Not Occur

  • Cenani Syndactylism

    In some fetuses, this process does not occur completely between all fingers or toes and some residual webbing remains.[en.academic.ru] The ulna and radius may be fused and shortened. The feet are usually less severely affected. Joint mobility may be restricted.[accessanesthesiology.mhmedical.com] bullosa with pyloric atresia EDAR ( EDAR Hypohidrotic ectodermal dysplasia ) · PTCH1 ( Nevoid basal cell carcinoma syndrome ) · BMPR1A ( BMPR1A Juvenile polyposis syndrome[dictionary.sensagent.com]

  • Herlitz Disease

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

    Missing: Fused Ulna and Radius
  • Syndactyly

    This condition does not have a notable cause and may occur in isolation or is inherited.[epainassist.com] The anomaly may involve radius and ulna that are either fused, short, or rudimentary resulting in luxation of the radial head and mesomelic shortening of forearm. 3 Lower[doi.org] Secondary syndactyly, also called "pseudosyndactyly", is rare and can be a complication of burns, dystrophic epidermolysis bullosa or trauma.[ncbi.nlm.nih.gov]

  • 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.[docplayer.net] bullosa H00584 Epidermolysis bullosa simplex H00585 Epidermolysis bullosa, hemidesmosomal H00586 Epidermolysis bullosa, junctional [PATH: hsa04510 hsa04512 hsa04514 hsa04810[genome.jp] 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.[vdocuments.mx]

    Missing: Fused Ulna and Radius
  • 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).[ncbi.nlm.nih.gov] Patients CMD with familial junctional epidermolysis bullosa often have brain atrophy and enlarged ventricles on MRI.[emedicine.medscape.com] 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.[emedicine.medscape.com]

    Missing: Fused Ulna and Radius Syndactyly Does Not Occur
  • Esophageal Stenosis

    Epidermolysis bullosa (EB) is a disease with 3 forms, most hereditary, characterized by spontaneous blistering lesions.[ncbi.nlm.nih.gov] We report a 13-year-old boy with recessive dystrophic epidermolysis bullosa who had dysphagia due to esophageal stenosis.[ncbi.nlm.nih.gov] Recessive dystrophic epidermolysis bullosa (RDEB) is an inherited disorder of squamous epithelium that results in dystrophic scarring of the skin after minor trauma.[ncbi.nlm.nih.gov]

    Missing: Fused Ulna and Radius Syndactyly Does Not Occur
  • Epidermolysis Bullosa Acquisita

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

    Missing: Fused Ulna and Radius Syndactyly Does Not Occur
  • Mucous Membrane Pemphigoid

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

    Missing: Fused Ulna and Radius Syndactyly Does Not Occur
  • Bullous Pemphigoid

    epidermolysis bullosa acquisita) or the epidermal side ('roof' for bullous pemphigoid) of the salt-split direct immunofluorescence specimen.[ncbi.nlm.nih.gov] bullosa.[ncbi.nlm.nih.gov] 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[icd10data.com]

    Missing: Fused Ulna and Radius Syndactyly Does Not Occur
  • Toxic Epidermal Necrolysis

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

    Missing: Fused Ulna and Radius Syndactyly Does Not Occur

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