Reference for MONILETHRIX. Search for MONILETHRIX

AI searches containing MONILETHRIX

MONILETHRIX

Monilethrix

Medical condition

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

Hair disease

Medical condition

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

Hair disease

Hair_disease

Keratin disease

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

Keratin_disease

Trichoscopy

Medical diagnostic method

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

Minoxidil

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

Dermatoscopy

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

Body odor

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

Body_odor

List of cutaneous conditions caused by problems with junctional proteins

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

Rodney Sinclair

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

Rodney_Sinclair

KRT86

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

List of genes mutated in cutaneous 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

List of skin conditions

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

List_of_skin_conditions

List of cutaneous conditions caused by mutations in keratins

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

KRT81

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

List of diseases (M)

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

List of diseases (M)

List_of_diseases_(M)

Pili torti

Medical condition

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

Pili torti

Pili_torti

Raymond Sabouraud

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

Raymond_Sabouraud

Lidia Rudnicka

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

Lidia_Rudnicka

KRT83

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

List of OMIM disorder codes

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

List of OMIM disorder codes

List_of_OMIM_disorder_codes

Online names & meanings

Cavendish

Surname or Lastname

English

Cavendish

English : habitational name from a place in Suffolk named Cavendish, from an Old English byname CÄfna (meaning â€˜boldâ€™, â€˜daringâ€™) + Old English edisc â€˜enclosed pastureâ€™.