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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[] Work-up revealed iron deficiency anemia, zinc deficiency and an abnormal celiac panel.[] Recurrent aphthous stomatitis was reported in 26 patients (53.0%) and in 13 (25.5%) controls ( p 0.005).[]

  • 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.[] Discovering genetic causes of zinc deficiency has been a remarkable scientific journey.[] 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[]

  • Congenital Leukonychia

    […] malformations Similars Q84.0 - Congenital alopecia Q84.1 - Congenital morphological disturbances of hair, not elsewhere classified Q84.2 - Other congenital malformations[] "Leukonychia on finger nails as a marker of calcium and/or zinc deficiency".[] (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[]

  • Zinc Deficiency

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

  • Immune System Disorder

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

  • Patterson Pseudoleprechaunism Syndrome

    alopecia, Stevanovic type - See Autosomal dominant palmoplantar keratoderma and congenital alopecia Palmoplantar keratoderma and sensorineural deafness - See Keratoderma[] 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[] stomatitis, pharyngitis and adenitis Periodontal disease / Periodontitis Peripartum cardiomyopathy Peripheral blood vessel disorder Peripheral nervous disorder Peripheral[]

  • 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[] Zinc deficiency is very common among the institutionalized elderly and homebound patients.[] stomatitis , and inflammatory bowel disease . [31] Malignancy In patients with CVID, the risk of certain malignancies is high.[]

  • Hereditary Mucoepithelial Dysplasia

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

  • 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[] 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[] stomatitis Aplasia cutis autosomal recessive Aplasia cutis congenita Aplasia cutis congenita dominant Aplasia cutis congenita intestinal lymphangiectasia Aplasia cutis congenita[]

  • Erythema Toxicum Neonatorum

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

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