Results 111 to 120 of about 596 (152)

Trichomycosis Axillaris: A Clinicoetiological Study. [PDF]

open access: yesIndian Dermatol Online J
Kalimuthu A   +3 more
europepmc   +1 more source

Gene detection in a family with monilethrix and treatment with 5% topical minoxidil [PDF]

open access: yesSkin Research and Technology, 2023
Abstract Objective To determine the causative gene mutation in a family with monilethrix and observe the therapeutic effect of 5% topical minoxidil. Method Clinical data from a family with monilethrix were collected. Peripheral blood samples were taken from the proband, the parents, and 100 unrelated healthy controls. Genomic DNA was extracted.
Pengqiang Du
exaly   +3 more sources

Monilethrix

open access: yesJAMA Dermatology
This case report describes sparse, unruly, fragile, and easily breakable hair, with patchy alopecia with diffuse follicular papules throughout the scalp as well as short hair with an alternation of darker elliptical nodes, with paler nonmedullated paler internodes giving a necklace appearance.
Piccolo V., Argenziano G.
openaire   +3 more sources

Monilethrix and Pseudo-Monilethrix

open access: yes, 1990
The name is derived from monile (Lat.) = necklace and thrix (Gk.) = hair to indicate a resemblance to a string of beads or a necklace (Fig. 1).
B. Bentley-Phillips
openaire   +2 more sources

Monilethrix Treated with Minoxidil [PDF]

open access: yesInternational Journal of Immunopathology and Pharmacology, 2011
In literature many different therapies are proposed to treat Monilethrix, but a definitive therapy still doe not exist. We decided to treat four patients affected by Monilethrix, with topical minoxidil 2%, 1 ml night and day for 1 year.
Alessandra Iorio   +2 more
exaly   +2 more sources

Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype [PDF]

open access: yesJournal of Investigative Dermatology, 1999
Monilethrix is an hereditary hair dystrophy recently shown to be due to mutations in the helix termination motif of two type II (basic) human hair keratin genes, hHb1 and hHb6. It has been suggested that mutation in hHb1 produces a less severe phenotype.
Eugene Healy   +2 more
exaly   +8 more sources

Home - About - Disclaimer - Privacy