Results 51 to 60 of about 596 (152)

The Role of Dermoscopy in the Management of Hair and Scalp Disorders: From Diagnosis to Therapeutic Monitoring

open access: yesDermatologic Therapy, Volume 2026, Issue 1, 2026.
Trichoscopy, the dermoscopic examination of hair and scalp, is an increasingly valuable tool in the management of hair and scalp disorders. Beyond its diagnostic utility, it is important for prognostic assessment and therapeutic monitoring. We conducted a literature search in Medline–PubMed and Scopus using the terms “trichoscopy,” “dermoscopy,” and ...
Anna Bolzon   +3 more
wiley   +1 more source

An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis [PDF]

open access: yes, 2006
Monilethrix is a structural defect of the hair shaft usually inherited in an autosomal dominant fashion and caused by mutations in the hHb1, hHb3, and hHb6 keratin genes. Autosomal recessive inheritance in this disease has been sporadically reported.
Marek, Dina   +10 more
core   +1 more source

Ultrastructural and clinical improvement in monilethrix treated with L-cystine

open access: yes, 1993
We report two childhood cases of monilethrix treated with L-cystine orally at a dose of 500 mg twice daily for 3 months. At the end of the treatment period clinical and ultrastructural improvements of the hair were recorded by scanning electron ...
M.Barbareschi   +3 more
core   +1 more source

Pathogenesis of Monilethrix: Computer Stereography and Electron Microscopy [PDF]

open access: yes, 1990
The plucked hairs and biopsied hair follicles of the scalp were obtained from a female patient with monilethrix. By scanning electron microscopy, the plucked hairs showed a typical moniliform feature composed of alternated nodes and inter- nodes.
Hashimoto, Ken   +3 more
core   +1 more source

Differential diagnostics of syphilitic alopecia and alopecia areata: The clinical picture and trichoscopic signs

open access: yesVestnik Dermatologii i Venerologii, 2019
This paper describes a clinical case of secondary syphilis, which was manifested exclusively by syphilitic alopecia.We describe the details of the clinical picture, as well as a differential diagnosis of syphilitic alopecia and alopecia areata on the ...
A. N. Mareeva   +2 more
doaj   +1 more source

In Vivo Imaging Techniques for the Human Scalp: A Systematic Review of the Literature

open access: yesLasers in Surgery and Medicine, Volume 56, Issue 9, Page 741-754, November 2024.
ABSTRACT Objective Scalp inflammation and alopecia are distressing conditions for which patients regularly present to dermatology. Although some diagnoses can be made clinically, others require biopsy, which carries the risk of pain, infection, bleeding, and scarring.
Bobak Hedayati   +6 more
wiley   +1 more source

Dermoscopy of congenital dermatoses in pediatric age group: An observational study

open access: yesIndian Journal of Paediatric Dermatology, 2019
Objective: To study dermoscopic (DS) patterns of various congenital dermatologic conditions affecting pediatric age group. Background: DS helps to fill gap between histopathology and gross examination, especially in children as they are noncooperative ...
Prachi Chetankumar Gajjar   +2 more
doaj   +1 more source

Monilethrix Presenting With Diffuse Fragile Hair in an Adult Female

open access: yes
JEADV Clinical Practice, EarlyView.
Mandy Robertson, Jeffrey Donovan
wiley   +1 more source

PITFALLS OF MAPPING A LARGE TURKISH CONSANGUINEOUS FAMILY WITH VERTICAL MONILETHRIX INHERITANCE

open access: yes, 2009
Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance: Monilethrix, a rare autosomal dominant disease characterized by hair fragility and follicular hyperkeratosis, is caused by mutations in three type It hair ...
BAHADIR, SAVAŞKAN CEM   +6 more
core   +2 more sources

More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players [PDF]

open access: yes, 2006
Monilethrix, an autosomal dominant human hair disorder, is caused by mutations in three type II hair cortex keratins. Rare cases of the disease with non-vertical transmission have now been found to overlap with localized autosomal recessive hypotrichosis.
Schweizer, Jurgen
core   +1 more source

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