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86 Possible Causes for Aphthous Stomatitis, Congenital Alopecia, Zinc Deficiency

  • Celiac Disease

    Congenital heart defects Primary biliary cirrhosis IgA deficiency Isolated hypertransaminasemia Recurrent aphthous stomatitis Myasthenia gravis Recurrent pericarditis Psoriasis[doi.org] Work-up revealed iron deficiency anemia, zinc deficiency and an abnormal celiac panel.[ncbi.nlm.nih.gov] Recurrent aphthous stomatitis was reported in 26 patients (53.0%) and in 13 (25.5%) controls ( p 0.005).[ncbi.nlm.nih.gov]

  • Brandt Syndrome

    Rupture of blisters expose the purulent eroded skin lesions. [1,2,4] Alopecia Diffuse hair loss in scalp, eye lashes and eye brows can be seen.[explainmedicine.com] Discovering genetic causes of zinc deficiency has been a remarkable scientific journey.[ncbi.nlm.nih.gov] It is characterized by inflammation of the skin (dermatitis) around bodily openings (periorificial) and the tips of fingers and toes (acral), hair loss (alopecia), and diarrhea[en.wikipedia.org]

  • Congenital Leukonychia

    […] malformations Similars Q84.0 - Congenital alopecia Q84.1 - Congenital morphological disturbances of hair, not elsewhere classified Q84.2 - Other congenital malformations[icd-code.org] "Leukonychia on finger nails as a marker of calcium and/or zinc deficiency".[en.wikipedia.org] (Table 3) In this study dermatologic disorders such as xeroasis, eczema, aphthous stomatitis, splinter hemorrhage, and onycholysis were more common in the HD group then in[woundsresearch.com]

  • Zinc Deficiency

    Malnutrition, prematurity, total parenteral nutrition dependence, and burns increase the demand for zinc, whereas congenital malabsorption syndromes represent clinical situations[ncbi.nlm.nih.gov] Diagnosis: Measuring the plasma zinc levels helps in diagnosis of zinc deficiency.[symptoma.com] CONCLUSION: These results suggest an association between zinc deficiency and recurrent aphthous stomatitis.[ncbi.nlm.nih.gov]

  • Immune System Disorder

    alopecia and nail dystrophy TARP syndrome Trichohepatoenteric syndrome Tumor necrosis factor receptor-associated periodic syndrome Twin to twin transfusion syndrome Vici[rarediseases.info.nih.gov] In that experiment pregnant mice were given a zinc-deficient diet.[diagnose-me.com] , lamellar type 4 LIPN Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis CLDN1 Ichthyosis, spastic quadriplegia, and mental retardation ELOVL4 Ichthyosis[centogene.com]

  • Patterson Pseudoleprechaunism Syndrome

    alopecia, Stevanovic type - See Autosomal dominant palmoplantar keratoderma and congenital alopecia Palmoplantar keratoderma and sensorineural deafness - See Keratoderma[herenciageneticayenfermedad.blogspot.com] However, it is not decided if vitamin C will be useful in regions with anticyclone ubiquity of iron and/or zinc deficiency as well as high H. pylori contamination rates. 6[cardinalpub.com] stomatitis, pharyngitis and adenitis Periodontal disease / Periodontitis Peripartum cardiomyopathy Peripheral blood vessel disorder Peripheral nervous disorder Peripheral[bioreference.net]

  • Primary Immune Deficiency Disorder

    alopecia, and nail dystrophy AR 6 6 FOXP3 Immunodysregulation, polyendocrinopathy, and enteropathy XL 28 93 G6PC3 Neutropenia, severe congenital, Dursun syndrome AR 11 37[blueprintgenetics.com] Zinc deficiency is very common among the institutionalized elderly and homebound patients.[merckmanuals.com] stomatitis , and inflammatory bowel disease . [31] Malignancy In patients with CVID, the risk of certain malignancies is high.[emedicine.medscape.com]

  • Hereditary Mucoepithelial Dysplasia

    Congenital alopecia involving the scalp, eyebrows and eyelashes is another essential cutaneous manifestation of IFAP (Figure 1A ).[ojrd.biomedcentral.com] IFAP syndrome is caused by deficiency in MBTPS2, an intramembrane zinc metalloprotease essential for cholesterol homeostasis and ER stress response.[ijpd.in] STOMATITIS BEHÇET¿S SYNDROME SARCOIDOSIS OROFACIAL GRANULOMATOSIS WEGENER¿S GRANULOMATOSIS ALLERGIC MUCOSAL REACTIONS TO SYSTEMIC DRUG ADMINISTRATION ALLERGIC CONTACT STOMATITIS[catdir.loc.gov]

  • Oculo-Osteo-Cutaneous Syndrome

    Alopecia 2 Palmoplantar Keratoderma and Congenital Alopecia, Autosomal Dominant Papillon-Lefevre Syndrome Pili Torti and Developmental Delay Pilodental Dysplasia with Refractive[nfed.org] deficiency type 0.298850 Aggressive systemic mastocytosis 0.2379 Chronic granulomatous disease 0.2328 Congenital factor X deficiency 0.298249 Ehlers-Danlos syndrome 0.2209916[documents.tips] stomatitis Aplasia cutis autosomal recessive Aplasia cutis congenita Aplasia cutis congenita dominant Aplasia cutis congenita intestinal lymphangiectasia Aplasia cutis congenita[rarediseases.annualcongress.com]

  • Erythema Toxicum Neonatorum

    Aplasia cutis contenita This is a group of heterogeneous diseases that is characterized by congenital focal absence of skin.[pedclerk.bsd.uchicago.edu] Conditions that need to be considered in the differential diagnosis include psoriasis, contact or irritant dermatitis, and zinc deficiency.[adhb.govt.nz] (ACUTE HERPETIC GINGIVO STOMATITIS) STOMATITIS, APHTHOUS (See APHTHOUS STOMATITIS) STREPTOCOCCAL PHARYNGITIS STREPTOCOCCAL VULVOVAGINITIS STURGE- WEBER SYNDROME (SWS, ENCEPHALOFACIAL[euro-libris.ro]

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