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1,908 Possible Causes for Caused by Mutation in the Syntaxin 1B Gene, Vitiligo

  • Alopecia Areata

    Vitiligo and alopecia areata are common autoimmune diseases of the skin.[ncbi.nlm.nih.gov] Vitiligo and alopecia areata are two cutaneous diseases believed to be primarily autoimmune in pathogenesis.[ncbi.nlm.nih.gov] KEYWORDS: alopecia areata; atopic dermatitis; comorbidities; epidemiology; vitiligo[ncbi.nlm.nih.gov]

    Missing: Caused by Mutation in the Syntaxin 1B Gene
  • Pernicious Anemia

    The case presented here is a woman who had a restoration of fertility after initiation of vitamin B12 treatment for vitiligo-associated pernicious anemia.[ncbi.nlm.nih.gov] Vitiligo is an acquired disease characterized by depigmentation of the skin due to destruction of melanocytes.[ncbi.nlm.nih.gov] A patient with a 46-year history of vitiligo who also presented rheumatoid arthritis and pernicious anemia is described.[ncbi.nlm.nih.gov]

    Missing: Caused by Mutation in the Syntaxin 1B Gene
  • Vitiligo

    vitiligo.[niams.nih.gov] What is vitiligo? Vitiligo (vit-ill-EYE-go) is a disorder that causes patches of skin to become white.[niams.nih.gov] Who gets vitiligo? Anyone can get vitiligo, but it is more noticeable on people with dark skin.[niams.nih.gov]

    Missing: Caused by Mutation in the Syntaxin 1B Gene
  • Addison's Disease

    Patient with Addison’s disease on a background of vitiligo (face). Figure 2. Patient with Addison’s disease on a background of vitiligo (hands).[bjgp.org] These include: Vitiligo The skin condition vitiligo can also appear simultaneously with idiopathic autoimmune Addison's disease.[news-medical.net] One such patient presented in Autumn 2013 (see Figures 1 and 2 demonstrating vitiligo of the face and hands).[bjgp.org]

    Missing: Caused by Mutation in the Syntaxin 1B Gene
  • Uveomeningoencephalitic Syndrome

    Cytokines: the yin and yang of vitiligo pathogenesis.[bioportfolio.com] Uveomeningoencephalitic Syndrome yourself 0 0 A Syndrome characterized by bilateral granulomatous Uveitis with Iritis and secondary Glaucoma, premature Alopecia, symmetrical Vitiligo[dictionary.university] Steroid ointment was unsuccessful against the vitiligo.[kyushu-u.pure.elsevier.com]

    Missing: Caused by Mutation in the Syntaxin 1B Gene
  • Rothmund Thomson Syndrome

    Idiopathic Guttate Hypomelanosis Laugier-Hunziker Syndrome Lentigo Melasma Ocular Manifestations of Albinism Pigmented Lesions of the Eyelid Postinflammatory Hyperpigmentation Vitiligo[dokterairlangga.com]

    Missing: Caused by Mutation in the Syntaxin 1B Gene
  • Turner Syndrome

    An association with many autoimmune diseases is described as well as skin diseases such as psoriasis, vitiligo and alopecia areata.[ncbi.nlm.nih.gov] 0011307 Strabismus Cross-eyed Squint Squint eyes [ more ] 0000486 Type II diabetes mellitus Noninsulin-dependent diabetes Type 2 diabetes Type II diabetes [ more ] 0005978 Vitiligo[rarediseases.info.nih.gov] Skin lymphoedema - hands, feet, neck (pterygium coli), pigmented naevi, telangiectasias, vitiligo, keloid, seborrhoeic dermatitis; increased body hair with alopecia.[patient.info]

    Missing: Caused by Mutation in the Syntaxin 1B Gene
  • Acute Hepatic Porphyria

    In two young patients with acute hepatic porphyria syndrome and persisting paralyses, which increased in intensity during intermittent occurring crisis, the activity of erythrocyte porphobilinogen synthase (delta-aminolevulinic acid dehydratase) was found to be considerably diminished, below 1% of the value of normal[…][ncbi.nlm.nih.gov]

    Missing: Caused by Mutation in the Syntaxin 1B Gene
  • Variegate Porphyria

    […] may be limited; that CLINUVEL may never file an NDA for SCENESSE regulatory approval in the US; that the Company may not be able to access adequate capital to advance its vitiligo[porfiria.org] It will also be the first experience of a 28-day dosing cycle in any porphyria, mirroring that used in our vitiligo program,” Dr Rodenburger said. – End – 1 SCENESSE (afamelanotide16mg[porfiria.org]

    Missing: Caused by Mutation in the Syntaxin 1B Gene
  • Porphyria Cutanea Tarda

    He reported a 25 year-old history of vitiligo upon exposure to sunlight.[ncbi.nlm.nih.gov] Jansen T, Megahed M, Hölzle E, Plewig G: Provocation of porphyria cutanea tarda by KUVA therapy of vitiligo. Acta Derm Venereol (Stockh) 1995;75:232–233.[karger.com]

    Missing: Caused by Mutation in the Syntaxin 1B Gene

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