Monilethrix (also referred to as beaded hair) is a rare autosomal dominant hair disease that results in short, fragile, broken hair that appears beaded...
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Hair disease (section Monilethrix)
hypertrichosis, hypotrichosis (alopecia), Menkes kinky hair syndrome, monilethrix, and piedra. Folliculitis is an inflammatory response that occurs in...
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abnormalities. It was shown that this method is especially helpful in diagnosing monilethrix, Netherton syndrome and other pediatric diseases. In 2008 the first atlas...
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Steatocystoma multiplex Vellus hair cyst 81 Monilethrix 82 Alopecia areata 83 Monilethrix 85 Pure hair–nail type of ectodermal dysplasia 86 Monilethrix...
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disorder of one of the keratin genes.[citation needed] An example is monilethrix. The first to be identified was epidermolysis bullosa simplex. Examples...
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KRTHB1 have been observed in patients with a rare dominant hair disease, monilethrix. GRCh38: Ensembl release 89: ENSG00000170442 – Ensembl, May 2017 GRCm38:...
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scalp diseases, such as alopecia areata, female androgenic alopecia, monilethrix, Netherton syndrome, and woolly hair syndrome. Dermoscopy of hair and...
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deficiency MOMO syndrome Mondini dysplasia Mondor's disease Monge's disease Monilethrix Monoamine oxidase A deficiency Monoclonal gammopathy of undetermined...
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undergo a color change when exposed to X-rays Sabouraud's syndrome: Monilethrix, a congenital disease with early progressive loss of hair Sabouraud–Noiré...
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planopilaris Lichen spinulosus Loose anagen syndrome Menkes kinky hair syndrome Monilethrix Parakeratosis pustulosa Pili (Pili annulati Pili bifurcati Pili multigemini...
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Melanonychia Menkes kinky hair syndrome (kinky hair disease, Menkes disease) Monilethrix (beaded hair) Muehrcke's nails (Muehrcke's lines) Nail–patella syndrome...
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Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions". Journal of Investigative Dermatology...
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multiplex Vellus hair cyst KRT81 Monilethrix KRT83 Monilethrix KRT85 Pure hair–nail type of ectodermal dysplasia KRT86 Monilethrix LMNA Laminin A/C Progeria...
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Desmoglein 4 Localized autosomal recessive hypotrichosis Autosomal recessive monilethrix Desmoplakin Striate palmoplantar keratoderma Carvajal syndrome Skin fragility–wooly...
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the hair cortex. Mutations in the KRT83 gene have been associated with monilethrix. GRCh38: Ensembl release 89: ENSG00000170523 – Ensembl, May 2017 GRCm38:...
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KRTHB6 have been observed in patients with a rare dominant hair disease, monilethrix. GRCh38: Ensembl release 89: ENSG00000205426 – Ensembl, May 2017 GRCm38:...
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evaluation in genetic hair shaft abnormalities such as Netherton syndrome, monilethrix, wooly hair syndrome, pili torti, pili annulati and trichothiodystrophy...
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cofactor deficiency, type C; 252150; GPHN Monilethrix; 158000; KRT81 Monilethrix; 158000; KRT83 Monilethrix; 158000; KRT86 Mononeuropathy of the median...
234 KB (18,877 words) - 15:43, 9 May 2024