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This study observed that among patients with COVID-19 who have hair disorders, telogen effluvium is common, and the presence of trichodynia may lead to earlier presentation.

This essay reviews issues related to telogen effluvium, including diagnosis, classification, and management, but it reports no new clinical findings.

This study found that chemotherapy for breast cancer initially reduced hair density and anagen hair rate, which then returned to baseline or higher, whereas tamoxifen did not significantly affect hair growth.

Different skin conditions show distinct types of vessel inflammation, a new quality of life index for vulval disease is reliable, a certain intrauterine system might be linked to chronic vaginal yeast infections, and oral minoxidil reduces hair loss in women.

This study found that most cases of telogen effluvium in Iraqi women had no clear triggering factor, although significant hair thinning was uncommon.

In this study, most Iraqi women with telogen effluvium had no identifiable triggers, though severe stress was noted in 21% of cases prior to the condition onset.

The study found that Temporal Triangular Alopecia often starts in early childhood, while Folliculitis Decalvans is characterized by tufted hairs and redness around hair follicles.

In this study of women with breast cancer, chemotherapy led to temporary alopecia and altered hair characteristics, impacting quality of life, while Tamoxifen showed minimal hair density changes.

This collection of case reports discusses various rare dermatological conditions, including alopecia totalis with amyloidosis and multiple myeloma, and provides descriptive insights without reporting new clinical findings.

Hand-foot-mouth disease may cause nail loss in children.

Hair casts are often mistaken for head lice, scalp pain in hair loss is linked to certain nerve factors, eyelash growth treatment is safe and effective, and nail shedding in children may follow hand-foot-mouth disease.

Two women lost hair after mesotherapy for hair loss, with one having permanent and the other temporary hair loss.

In this study, researchers found that the prevalent Glu 410 Lys mutation in hHb6 and a new Glu 403 Lys mutation in hHb1 are linked to monilethrix, suggesting a mutational hotspot in type II hair keratins.

This study discusses trichodynia, a painful scalp condition often linked to various forms of alopecia and psychiatric comorbidities, highlighting its clinical diagnosis, lack of specific treatments, and suggesting the need for more research to explore effective therapies.

The algae grew better and fixed nitrogen more efficiently when they worked together, using nitrogen and iron.

This thesis reveals that tenuazonic acid inhibits plant plasma membrane H+-ATPase, suggesting its potential as a herbicide due to its impact on root elongation and cell viability in Arabidopsis thaliana.

This study found that trichothiodystrophic hair shows reduced and disoriented protein deposition in follicles, with both the cuticle and cortex affected, providing localized structural insights into keratin abnormalities.

This report describes a patient with trichothiodystrophy exhibiting both specific hair abnormalities and developmental delay, contributing to the understanding of this rare disorder's clinical presentation.

This abstract provides no results; it is a website notification about cookies and general access to JAMA content.

This case report describes a patient with lichen nitidus whose lesions improved following treatment with oral astemizole and topical steroids, although spontaneous resolution remains a possibility.

This article reviews the use of trichoscopy for diagnosing and monitoring various scalp conditions, but it presents no new experimental findings; the authors emphasize its precision in noninvasive evaluation.

In this study, the varied phenotype of trichothiodystrophy was highlighted, with findings of distinctive hair shaft abnormalities and a wide range of multisystem issues, including neurologic and urologic disorders.

This case report describes a 2-year-old boy diagnosed with trichothiodystrophy, characterized by fragile hair, intellectual damage, diminished fertility, and short stature.

This article discusses monilethrix, a rare human hair dysplasia caused by mutations in hair keratins, but reports no new clinical findings.

This study identified several specific trichoscopic features of trichotillomania, with trichoptilosis, V hair, and hair powder being the most frequent findings.

This case study observed that in a child with spontaneous trichonodosis, topical minoxidil and gentle hair care improved hair length and strength over two years, suggesting a potential genetic predisposition for the disorder.

In this study, most hair disorders among HIV-1 positive patients were associated with low helper T cell counts, with papulosquamous conditions like seborrheic dermatitis and psoriasis being the most common.

This article reviews the genetic and phenotypic characteristics of Trichothiodystrophy and discusses the associated DNA repair defects, but does not report new clinical findings.

This report describes a case where a sex reassignment patient on estrogen therapy experienced complete hair regrowth on a previously fully alopecic scalp.