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412 Possible Causes for Congenital Alopecia, Vitiligo

  • Alopecia

    463–469, AUG 2016 DOI: 10.1097/MOP.0000000000000375, PMID: 27191524 Issn Print: 1040-8703 Publication Date: 2016/08/01 Checking for direct PDF access through Ovid Abstract Vitiligo[doi.org] Congenital triangular alopecia Congenital triangular alopecia references Congenital triangular alopecia Congenital triangular alopecia is a patch of hair loss in the temple[keratin.com] Clinical presentations of vitiligo and alopecia areata A-B) Common vitiligo on the anticubital fossa and extensor knees of a 9-year-old male; C) Segmental vitiligo in a 15[ncbi.nlm.nih.gov]

  • Alopecia Areata

    Vitiligo and alopecia areata are common autoimmune diseases of the skin.[ncbi.nlm.nih.gov] We report 4 cases of congenital alopecia areata with follow-up from 3 to 5 years. The diagnosis was made clinically in all cases.[ncbi.nlm.nih.gov] During the first appointment, diagnoses of alopecia areata and congenital triangular alopecia were made. After one year, there was no change.[ncbi.nlm.nih.gov]

  • 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] Alopecia Syndrome Other Disorders of Keratinization Porokeratoses Kyrle’s Disease Pityriasis Rubra Pilaris Poikilodermas and Aging Syndromes Disorders of DNA Repair Aging[amazon.it] 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]

  • Rothmund Thomson Syndrome

    ; dystrophic nails - photosensitivity - congenital skeletal defects - hypoplasia or absence of the radii and thumbs, osteopenia, cystic or sclerotic changes of the long bones[atlasgeneticsoncology.org] Children with RTS may have sparse scalp hair or even total alopecia. Eyelashes and/or eyebrows may also be sparse or absent. Growth.[ncbi.nlm.nih.gov] […] year of life (90%) and persisting throuhout life: atrophic dermatosis, poikiloderma, hyperpigmentation, teleangiectasia - sparse hair which may progress to partial or total alopecia[atlasgeneticsoncology.org]

  • Congenital Alopecia

    And these drugs may help with vitiligo, a disease that causes pigment loss, leaving white spots on the skin.[yalemedicine.org] We present the first case of cutaneous mastocytosis associated with congenital alopecia areata in a 3-year-old Korean girl.[ncbi.nlm.nih.gov] ( 2061445 ) Tosti A....Guerra L. 1991 37 Alopecia totalis and vitiligo in common variable immunodeficiency. ( 2062780 ) Spickett G....Chapel H. 1991 38 Thyroid antibodies[malacards.org]

  • Atrichia with Papular Lesions

    alopecia, termed alopecia universalis congenita.[ncbi.nlm.nih.gov] […] information on serological diagnosis of pemphigus, TNF-I for hidradenitis suppurativa, the use of immunosuppressives for atopic dermatitis, excimer laser for the treatment of vitiligo[books.google.es] Noncultured epidermal suspension is usually performed in patients with vitiligo with duration of clinical stability (DS) of 12 months or longer because DS is a vital parameter[allmedx.com]

  • Alopecia Universalis

    We report a case of an unknown clinical combination of PCT with autoimmune hypothyroidism, alopecia universalis and vitiligo with thyroid and parietal cell circulating antibodies[ncbi.nlm.nih.gov] The skin biopsy ruled out congenital atrichia and was suggestive of alopecia areata.[ijtrichology.com] Those with vitiligo (patchy loss of skin color) may also develop alopecia universalis in time.[streetdirectory.com]

  • Alopecia Totalis

    No mention of congenital familial alopecia is made in his text. Sutton 2 mentioned congenital alopecia as a rare condition usually associated with other defects.[jamanetwork.com] Two of these patients had vitiligo. None of 20 healthy control sera stained the keratinocyte cells or the melanocyte nuclei.[ncbi.nlm.nih.gov] […] which results in premature induction of anagen follicles to catagen and telogen, without causing destruction of the hair follicle.¹ This mechanism is similar to that of vitiligo[my.clevelandclinic.org]

  • Congenital Leukonychia

    Raindrop Hypopigmentation Subungual Exostoses T-cell immunodeficiency, congenital alopecia, and nail dystrophy tinea favosa tinea unguium Trichoodontoonychial Dysplasia vitiligo[rgd.mcw.edu] […] malformations Similars Q84.0 - Congenital alopecia Q84.1 - Congenital morphological disturbances of hair, not elsewhere classified Q84.2 - Other congenital malformations[icd-code.org] […] dysplasia Darier's disease Fever Hypoalbuminemia Iron deficiency Leprosy Malabsorption Mycosis Nitrate solution Silver solution Sulphonamides Noxa Steatocystoma multiplex Trauma Vitiligo[wikidoc.org]

  • Autoimmune Adrenal Insufficiency

    See glucocorticoid, mineralocorticoid, androgen. adrenal cortex inhibitors adrenal cortical dysfunction adrenal hyperplasia-like syndrome a congenital abnormality of adrenal[medical-dictionary.thefreedictionary.com] The main autoimmune diseases in AD: thyroid diseases – 34%, premature ovarian failure (POF) – 14%, IDDM and vitiligo – 13%, while in SAI – 36, 4, 3 and 4% respectively.[endocrine-abstracts.org] Thyroid disease was most common (47%), followed by type 1 diabetes (12%), vitiligo (11%), vitamin B12 deficiency (10%), and premature ovarian insufficiency (6.6% of women)[portal.research.lu.se]

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