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350 Possible Causes for Congenital Alopecia, Hypothyroidism, Vitiligo

  • Alopecia Areata

    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] Hypothyroidism can develop in patients with Graves' disease, either spontaneously or as a result of radioactive iodine therapy or surgery.[ncbi.nlm.nih.gov] Vitiligo and alopecia areata are common autoimmune diseases of the skin.[ncbi.nlm.nih.gov]

  • Alopecia

    Congenital triangular alopecia Congenital triangular alopecia references Congenital triangular alopecia Congenital triangular alopecia is a patch of hair loss in the temple[keratin.com] A 22-year-old hypothyroid girl underwent right radical nephrectomy for T2N0 RCC. Histopathology was clear cell carcinoma.[ncbi.nlm.nih.gov] 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]

  • Hypothyroidism

    […] of the puppy coat, hyperpigmentation of the skin, and bilaterally symmetric alopecia of the trunk.[web.archive.org] On this page: What is hypothyroidism? What is the thyroid? What causes hypothyroidism? What are the symptoms of hypothyroidism? Who is likely to develop hypothyroidism?[web.archive.org] Prematurely graying hair Autoimmune disorders such as type 1 diabetes, multiple sclerosis, rheumatoid arthritis, celiac disease, Addison's disease, pernicious anemia, or vitiligo[webmd.com]

  • Secondary Hypothyroidism

    Alopecia, weight gain, mental dullness, fatigue, cold intolerance, infertility and neurological deficits are seen.[medical-dictionary.thefreedictionary.com] Clinical presentation of a hypothyroid state differs by some factors.[symptoma.com] Prematurely graying hair Autoimmune disorders such as type 1 diabetes, multiple sclerosis, rheumatoid arthritis, celiac disease, Addison's disease, pernicious anemia, or vitiligo[webmd.com]

  • 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] ) with an associated mild hypothyroidism.[autoimmunephoenix.wordpress.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]

  • 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] […] symptomatic primary biliary cirrhosis 無症候性原発性胆汁性肝硬変 asymptomatic primary biliary cirrhosis 硬化性胆管炎 sclerosing cholangitis 膠原病 collagen disease 甲状腺機能亢進症 hyperthyroidism 甲状腺機能低下症 hypothyroidism[jsge.or.jp]

  • Ichthyosis

    , autosomal recessive 9 CLDN1 Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis CYP4F22 Ichthyosis, congenital, autosomal recessive 5 EBP Chondrodysplasia[asperbio.com] […] certain forms of malignant disease and infectious disease, in dietary and vitamin A deficiencies, as a side effect of cholesterol-lowering medication, in dialysis patients, hypothyroidism[nativeremedies.com] […] n JM 2018 46 Porphyria Cutanea Tarda Presenting with Scleroderma, Ichthyosis, Alopecia, and Vitiligo. ( 29928199 ) MacGillivray ME...Salopek TG 2018 47 Identification of mutations[malacards.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] In addition to the Rothmund-Thomson syndrome, her medical history was significant for a history of hypothyroidism and pituitary insufficiency for which she received injections[healio.com] 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]

  • Tollner-Horst-Manzke Syndrome

    Alopecia epilepsy oligophrenia syndrome of Moynahan Alopecia intellectual disability syndrome 2 Alopecia totalis Alopecia universalis Alopecia universalis onychodystrophy vitiligo[rarediseases.info.nih.gov] Fragility Hypogonadism with Low-Grade Mental Deficiency and Microcephaly hypogonadotropic hypogonadism 23 with or without anosmia Hypohidrotic Ectodermal Dysplasia, with Hypothyroidism[rgd.mcw.edu] alopecia Autosomal dominant partial epilepsy with auditory features Autosomal dominant polycystic kidney disease - Not a rare disease Autosomal dominant pseudohypoaldosteronism[rarediseases.info.nih.gov]

  • Adrenal Insufficiency

    Clinical signs include bilaterally symmetrical alopecia resembling that seen with other endocrinopathies. adrenal insufficiency hypofunction of the adrenal gland, particularly[medical-dictionary.thefreedictionary.com] Basal hormone levels and pituitary function tests indicated secondary hypothyroidism and adrenal insufficiency due to hypopituitarism.[ncbi.nlm.nih.gov] […] situation may be associated with symptoms suggestive of chronic adrenal insufficiency such as hyperpigmentation, salt craving, and association with autoimmune diseases such as vitiligo[ncbi.nlm.nih.gov]

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