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Genetic disorder resulting in short, brittle, beaded hair
Monilethrix (also referred to as beaded hair) is a rare autosomal dominant hair disease that results in short, fragile, broken hair that appears beaded
Monilethrix
Medical condition
hypertrichosis, hypotrichosis (alopecia), Menkes kinky hair syndrome, monilethrix, and piedra. Folliculitis is an inflammatory response that occurs in
Hair_disease
Medical examination technique of the hair and scalp
abnormalities. It was shown that this method is especially helpful in diagnosing monilethrix, Netherton syndrome and other pediatric diseases. In 2008 the first atlas
Trichoscopy
Medical condition
disorder of one of the keratin genes.[citation needed] An example is monilethrix. The first to be identified was epidermolysis bullosa simplex. Examples
Keratin_disease
Medication to treat high blood pressure and alopecia
1111/ajd.12350. PMID 25966934. Sinclair R (May 2016). "Treatment of monilethrix with oral minoxidil". JAAD Case Reports. 2 (3): 212–215. doi:10.1016/j
Minoxidil
Protein-coding gene in the species Homo sapiens
KRT81 have been observed in patients with a rare dominant hair disease, monilethrix. GRCh38: Ensembl release 89: ENSG00000170442 – Ensembl, May 2017 GRCm38:
KRT86
Steatocystoma multiplex Vellus hair cyst 81 Monilethrix 82 Alopecia areata 83 Monilethrix 85 Pure hair–nail type of ectodermal dysplasia 86 Monilethrix
List of cutaneous conditions caused by mutations in keratins
List_of_cutaneous_conditions_caused_by_mutations_in_keratins
Medical examination of the skin
scalp diseases, such as alopecia areata, female androgenic alopecia, monilethrix, Netherton syndrome, and woolly hair syndrome. Dermoscopy of hair and
Dermatoscopy
1111/ajd.12350. PMID 25966934. Sinclair R (May 2016). "Treatment of monilethrix with oral minoxidil". JAAD Case Rep. 2 (3): 212–215. doi:10.1016/j.jdcr
Rodney_Sinclair
Desmoglein 4 Localized autosomal recessive hypotrichosis Autosomal recessive monilethrix Desmoplakin Striate palmoplantar keratoderma Carvajal syndrome Skin fragility–wooly
List of cutaneous conditions caused by problems with junctional proteins
List_of_cutaneous_conditions_caused_by_problems_with_junctional_proteins
Odor produced by a living animal
planopilaris Lichen spinulosus Loose anagen syndrome Menkes kinky hair syndrome Monilethrix Parakeratosis pustulosa Pili (Pili annulati Pili bifurcati Pili multigemini
Body_odor
Melanonychia Menkes kinky hair syndrome (kinky hair disease, Menkes disease) Monilethrix (beaded hair) Muehrcke's nails (Muehrcke's lines) Nail–patella syndrome
List_of_skin_conditions
multiplex Vellus hair cyst KRT81 Monilethrix KRT83 Monilethrix KRT85 Pure hair–nail type of ectodermal dysplasia KRT86 Monilethrix LMNA Laminin A/C Progeria
List of genes mutated in cutaneous conditions
List_of_genes_mutated_in_cutaneous_conditions
Medical condition
Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions". Journal of Investigative Dermatology
Pili_torti
Protein-coding gene in the species Homo sapiens
KRTHB6 have been observed in patients with a rare dominant hair disease, monilethrix. GRCh38: Ensembl release 89: ENSG00000205426 – Ensembl, May 2017 GRCm38:
KRT81
Protein-coding gene in Homo sapiens
the hair cortex. Mutations in the KRT83 gene have been associated with monilethrix. GRCh38: Ensembl release 89: ENSG00000170523 – Ensembl, May 2017 GRCm38:
KRT83
French physician
undergo a color change when exposed to X-rays Sabouraud's syndrome: Monilethrix, a congenital disease with early progressive loss of hair Sabouraud–Noiré
Raymond_Sabouraud
deficiency MOMO syndrome Mondini dysplasia Mondor's disease Monge's disease Monilethrix Monoamine oxidase A deficiency Monoclonal gammopathy of undetermined
List_of_diseases_(M)
Polish-American dermatologist
evaluation in genetic hair shaft abnormalities such as Netherton syndrome, monilethrix, wooly hair syndrome, pili torti, pili annulati and trichothiodystrophy
Lidia_Rudnicka
cofactor deficiency, type C; 252150; GPHN Monilethrix; 158000; KRT81 Monilethrix; 158000; KRT83 Monilethrix; 158000; KRT86 Mononeuropathy of the median
List_of_OMIM_disorder_codes
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