Monilethrix (also referred to as beaded hair) is a rare autosomal dominant hair disease that results in short, fragile, broken hair that appears beaded...

hypertrichosis, hypotrichosis (alopecia), Menkes kinky hair syndrome, monilethrix, and piedra. Folliculitis is an inflammatory response that occurs in...

abnormalities. It was shown that this method is especially helpful in diagnosing monilethrix, Netherton syndrome and other pediatric diseases. In 2008 the first atlas...

Steatocystoma multiplex Vellus hair cyst 81 Monilethrix 82 Alopecia areata 83 Monilethrix 85 Pure hair–nail type of ectodermal dysplasia 86 Monilethrix...

disorder of one of the keratin genes.[citation needed] An example is monilethrix. The first to be identified was epidermolysis bullosa simplex. Examples...

KRTHB1 have been observed in patients with a rare dominant hair disease, monilethrix. GRCh38: Ensembl release 89: ENSG00000170442 – Ensembl, May 2017 GRCm38:...

scalp diseases, such as alopecia areata, female androgenic alopecia, monilethrix, Netherton syndrome, and woolly hair syndrome. Dermoscopy of hair and...

deficiency MOMO syndrome Mondini dysplasia Mondor's disease Monge's disease Monilethrix Monoamine oxidase A deficiency Monoclonal gammopathy of undetermined...

undergo a color change when exposed to X-rays Sabouraud's syndrome: Monilethrix, a congenital disease with early progressive loss of hair Sabouraud–Noiré...

planopilaris Lichen spinulosus Loose anagen syndrome Menkes kinky hair syndrome Monilethrix Parakeratosis pustulosa Pili (Pili annulati Pili bifurcati Pili multigemini...

Melanonychia Menkes kinky hair syndrome (kinky hair disease, Menkes disease) Monilethrix (beaded hair) Muehrcke's nails (Muehrcke's lines) Nail–patella syndrome...

Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions". Journal of Investigative Dermatology...

multiplex Vellus hair cyst KRT81 Monilethrix KRT83 Monilethrix KRT85 Pure hair–nail type of ectodermal dysplasia KRT86 Monilethrix LMNA Laminin A/C Progeria...

Desmoglein 4 Localized autosomal recessive hypotrichosis Autosomal recessive monilethrix Desmoplakin Striate palmoplantar keratoderma Carvajal syndrome Skin fragility–wooly...

the hair cortex. Mutations in the KRT83 gene have been associated with monilethrix. GRCh38: Ensembl release 89: ENSG00000170523 – Ensembl, May 2017 GRCm38:...

KRTHB6 have been observed in patients with a rare dominant hair disease, monilethrix. GRCh38: Ensembl release 89: ENSG00000205426 – Ensembl, May 2017 GRCm38:...

evaluation in genetic hair shaft abnormalities such as Netherton syndrome, monilethrix, wooly hair syndrome, pili torti, pili annulati and trichothiodystrophy...

cofactor deficiency, type C; 252150; GPHN Monilethrix; 158000; KRT81 Monilethrix; 158000; KRT83 Monilethrix; 158000; KRT86 Mononeuropathy of the median...