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10 Possible Causes for Congenital Alopecia Universalis, Reiter's Syndrome

  • Dystrophic Nail

    Available from: Congenital alopecia universalis is one of the rarest anomaly which involves skin and appendages.[ijtrichology.com] The skin biopsy ruled out congenital atrichia and was suggestive of alopecia areata.[ijtrichology.com] alopecia universalis is one of the rarest anomaly which involves skin and appendages.[ijtrichology.com]

  • FLOTCH Syndrome

    […] arthritis, Leprosy, Loeys-dietz syndrome, Myelofibrosis, Neurofibromatosis, Pseudoxanthoma elasticum, Reiter’s syndrome, Rheumatic fever Sexual Congenital herpes simplex Trauma[wikidoc.org] Various causes for diffuse hair loss like alopecia universalis, congenital atrichia with papular lesions, systemic lupus erythematosus, alopecia neoplastica (associated with[ijdvl.com] , Anaphylaxis, Celiac disease, Chediak-higashi syndrome, Cold autoimmune hemolytic anemia, Collagenous celiac disease, Drug allergies, Felty syndrome, Juvenile rheumatoid[wikidoc.org]

  • Strudwick Syndrome

    , polymyalgia rheumatica, primary agammaglobulinemia, primary biliary cirrhosis, psoriasis, Raynaud's phenomena, Reiter's syndrome, rheumatoid arthritis (RA), Sjorgen's syndrome[lens.org] universalis; Alpha-1 -antichymotrypsin deficiency; Alpha-methylacyl-CoA racemase deficiency; Alpha-thalassemia/mental retardation syndrome; Alport syndrome; Alzheimer disease[lens.org] […] leprosy, listeriosis, pneumonia, meningitis, bacterial meningitis, anthrax, otitis media, Mycoplasma hominis, neonatal sepsis (Chorioamnionitis), noma, paratyphus, plague, Reiter's[lens.org]

  • Isolated Toenail Dystrophy

    Onycholysis Psoriasis, infection, hyperthyroidism, sarcoidosis, trauma, amyloidosis, connective tissue disorders Pitting Psoriasis, Reiter’s syndrome, incontinentia pigmenti[aafp.org] Available from: Congenital alopecia universalis is one of the rarest anomaly which involves skin and appendages.[ijtrichology.com] ’s syndrome (a type of arthritis that develops in response to an infection in another part of the body) and other connective tissue disorders Sarcoidosis (a disease in which[wholehealthinsider.com]

  • Thumb Deformity - Alopecia - Pigmentation Anomaly Syndrome

    Figure 10-30: (Plate 37) Hyperkeratotic lesions encrusted on the soles of the feet in Reiter's syndrome.[arthritisresearch.us] Alopecia, epilepsy, pyorrhea, mental subnormality 0 *Alopecia/congenital *Epilepsy *Intellectual Disability *Craniofacial Abnormalities.[reference.md] Disorders Associated with Pericardial Disease Pericarditis may be a result of Reiter's syndrome, Whipple's disease, Kawasaki's disease, SLE, rheumatoid arthritis,![arthritisresearch.us]

  • Zlotogora-Ogur Syndrome

    , polymyalgia rheumatica, primary agammaglobulinemia, primary biliary cirrhosis, psoriasis, Raynaud's phenomena, Reiter's syndrome, rheumatoid arthritis (RA), Sjorgen's syndrome[lens.org] universalis; Alpha-1 -antichymotrypsin deficiency; Alpha-methylacyl-CoA racemase deficiency; Alpha-thalassemia/mental retardation syndrome; Alport syndrome; Alzheimer disease[lens.org] […] leprosy, listeriosis, pneumonia, meningitis, bacterial meningitis, anthrax, otitis media, Mycoplasma hominis, neonatal sepsis (Chorioamnionitis), noma, paratyphus, plague, Reiter's[lens.org]

  • Spondylometaphyseal Dysplasia with Combined Immunodeficiency

    , polymyalgia rheumatica, primary agammaglobulinemia, primary biliary cirrhosis, psoriasis, Raynaud's phenomena, Reiter's syndrome, rheumatoid arthritis (RA), Sjorgen's syndrome[lens.org] universalis; Alpha-1 -antichymotrypsin deficiency; Alpha-methylacyl-CoA racemase deficiency; Alpha-thalassemia/mental retardation syndrome; Alport syndrome; Alzheimer disease[lens.org] […] leprosy, listeriosis, pneumonia, meningitis, bacterial meningitis, anthrax, otitis media, Mycoplasma hominis, neonatal sepsis (Chorioamnionitis), noma, paratyphus, plague, Reiter's[lens.org]

  • Pachyonychia Congenita, Type 2

    , polymyalgia rheumatica, primary agammaglobulinemia, primary biliary cirrhosis, psoriasis, Raynaud's phenomena, Reiter's syndrome, rheumatoid arthritis (RA), Sjorgen's syndrome[lens.org] universalis; Alpha-1 -antichymotrypsin deficiency; Alpha-methylacyl-CoA racemase deficiency; Alpha-thalassemia/mental retardation syndrome; Alport syndrome; Alzheimer disease[lens.org] […] leprosy, listeriosis, pneumonia, meningitis, bacterial meningitis, anthrax, otitis media, Mycoplasma hominis, neonatal sepsis (Chorioamnionitis), noma, paratyphus, plague, Reiter's[lens.org]

  • X-linked Intellectual Disability Type Kroes

    Saraiva JM, Baraitser M (1992) Joubert syndrome: a review. Am J Med Genet 43:726–731 PubMed CrossRef 57.[springermedizin.de] universalis 253375 Trisomy X 42.5 94058 Neovascular glaucoma 24.4801 Scleroderma 42 1199 Esophageal atresia 24.3217071 Non-familial renal cell carcinoma 42 3318 Essential[fliphtml5.com] Singla V, Romaguera-Ros M, Garcia-Verdugo JM, Reiter JF (2010) Ofd1, a human disease gene, regulates the length and distal structure of centrioles.[springermedizin.de]

  • Al-Gazali-Dattani Syndrome

    Mannose corrects altered N-glycosylation in carbohydrate-deficient glycoprotein syndrome fibroblasts.[ajpediatrics.org] universalis 253375 Trisomy X 42.5 94058 Neovascular glaucoma 24.4801 Scleroderma 42 1199 Esophageal atresia 24.3217071 Non-familial renal cell carcinoma 42 3318 Essential[fliphtml5.com] Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.[ajpediatrics.org]

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