Create issue ticket

33 Possible Causes for Brandt Syndrome, Congenital Alopecia, Vitiligo

  • Zinc Deficiency

    A wide variety of persistent skin problems such as stretch marks, rashes, seborrheic dermatitis, eczema , psoriasis , fine varicose veins, boils, vitiligo and skin infections[growyouthful.com] Malnutrition, prematurity, total parenteral nutrition dependence, and burns increase the demand for zinc, whereas congenital malabsorption syndromes represent clinical situations[ncbi.nlm.nih.gov] It is also called acrodermatitis enteropathy, primary zinc malabsorption syndrome, Danbolt-Closs syndrome and Brandt syndrome.[dermnetnz.org]

  • Chilblain Lupus Erythematosus

    […] is a rare presentation of lupus erythematosus that may simulate vitiligo.[ucdavis.pure.elsevier.com] We report a very unusual case of NLE that was characterized by congenital skin atrophy, erosions, alopecia, and profound pancytopenia.[thedoctorsdoctor.com] syndromes in pediatric onset systemic lupus erythematosus.[ped-rheum.biomedcentral.com]

  • Bangstad Syndrome

    Narrow mouth Congenital generalized lipodystrophy Proptosis Retrognathia Decreased fertility in females Thick hair Bone cyst Sparse hair Abnormality of skin pigmentation[mendelian.co] Brandt J, Wong C, Mihm S, Roberts J, Smith J, Brewer E, et al. Invasive pneumococcal disease and hemolytic uremic syndrome. Pediatrics. 2002;110:371–6.[springermedizin.de] […] common systemic autoimmune diseases include rheumatoid arthritis , systemic lupus erythematosus, diabetes mellitus, Sjogren syndrome, scleroderma , Goodpasture syndrome, vitiligo[medicinenet.com]

  • 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] 170 Branched-Chain Ketoaciduria 171 Branchial Clefts with Characteristic Facies , Growth Retardation, Imperforate Nasolacrimal Duct, and Premature Aging 172 Brandt Syndrome[dentisty.org] […] visionww@aol.com 1,2,5 VITAMIN B12 METABOLISM; INBORN ERROR OF See: Cobalamin (B12) Defiency VITILIGO The Canadian Vitiligo Society Dr.[thefreelibrary.com]

  • Hypertrichosis

    […] hair Congenital alopecia Congenital alopecia with keratin cysts Congenital anomaly of hair Congenital beaded hair Congenital generalized alopecia Congenital hair anomaly[icd9data.com] (Beighton, 1970; Brandt, 1897; Broster, 1950; Cantu, 1982; Demikova, 1986; Felgenhauer, 1969; Freire-Maia, 1976; Gardner, 1964; Jalili, 1989; Janssen, 1945; Joest, 1984; Judge[hairscientists.org] The association of acquired hypertrichosis lanuginosa and vitiligo has not been reported in earlier reviews. [2], [4] We propose to add vitiligo to the list of associated[ijdvl.com]

  • Rasmussen Syndrome

    A 9-year-old boy diagnosed as having Rasmussen syndrome had congenital IgA deficiency and juvenile alopecia.[ncbi.nlm.nih.gov] Vinning EP, Freeman JM, Brandt J, Carson BS, Uematsu S: Progressive unilateral encephalopathy of childhood (Rasmussen’s syndrome): A reappraisal.[karger.com] Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic report.[doi.org]

  • Amaurosis-Hypertrichosis Syndrome

    […] megalocornea Stickler syndrome, type 2 Pitt-Hopkins syndrome Alopecia macular degeneration growth retardation Glycogen storage disease type 5 Hyperlipoproteinemia type 5[checkrare.com] Manifestations of Hirsutism Dermatologic Manifestations of Rubinstein-Taybi Syndrome Mucopolysaccharidoses Types I-VII Brandt A.[emedicine.medscape.com] […] areata, nodulocystic acne, granuloma annulare, granuloma faciale, hidradenitis suppurativa, localized and nail psoriasis, prurigo nodularis, cutaneous lupus erythematosus, vitiligo[ijdvl.com]

  • Lymphoma

    ) 090.9 acquired 097.9 alopecia (secondary) 091.82 anemia 095.8 aneurysm (artery) (ruptured) 093.89 aorta 093.0 central nervous system 094.89 congenital 090.5 anus 095.8 primary[theodora.com] Vertigo Aural Vesication VesicoUreteral Reflux Vestibular Neuronitis Viral Meningitis Comprehensive Includes Ebola Rhinoviruses Rotaviruses Influenza Vision Visual Vitamin Vitiligo[i2i.gi] , psycho-organic) 310.9 psychotic (see also Psychosis, organic) 294.9 senile (see also Dementia, senile) 290.0 branchial arch 744.41 Brandt's (acrodermatitis enteropathica[theodora.com]

  • Bonnemann-Meinecke-Reich Syndrome

    Dysplasia , Maroteaux Type Acroosteolysis Dominant Type Acrorenal-Mandibular Syndrome Adrenoleukodystrophy , Autosomal Neonatal Form Agenesis Of The Corpus Callosum And Congenital[familydiagnosis.com] - See Brachioskeletogenital syndrome Branchio-skeleto-genital syndrome - See Brachioskeletogenital syndrome Brandt syndrome - See Acrodermatitis enteropathica Brandywine[herenciageneticayenfermedad.blogspot.com] […] vestibulocochlear, vetebral, vi, vii, viii, viljoen, villonodular, villous, vipoma, viral, virilizing, virus, visceral, viscerum-cardiopathy, vitale, vitamin, vitamine, vitiligo[rapsodyonline.eurordis.org]

  • Cobb Syndrome

    Vitiligo. This autoimmune disease causes pigment losses in your skin, where you may have noticeable white patches.[healthline.com] Adrenal Hyperplasia (CAH) Congenital Alopecia Totalis Congenital Anodontia Congenital Cerebellum Hyperplasia Congenital Cone Dystrophy Congenital Cyto Megalovirus Congenital[geneticalliance.org.au] The silent sinus syndrome is a form of chronic maxillary atelectasis: A systematic review of all reported cases.[eyewiki.aao.org]

Similar symptoms