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A 14-year-old girl with a condition that makes her hair easy to pull out also has a hair-pulling disorder, and treatment helped but she relapsed after a year.

Recognizing Jacquet's sign helps diagnose and treat traction alopecia accurately.

Folliculotropic mycosis fungoides can look like alopecia areata.

Certain gene variations and low adiponectin levels may increase the risk of hair loss in Egyptians.

Some people with congenital triangular alopecia have a central tuft of hair in the bald patch, but the cause is unknown.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Sterilize stray dogs to prevent disease spread to wildlife.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Monilethrix is linked to a gene cluster on chromosome 12.

Persistent pulling on hair can cause permanent hair loss.

Less than a quarter of alopecia areata cases were unusual forms or had paradoxical regrowth.

Recognizing the "bamboo hair defect" is crucial for diagnosing Netherton's syndrome.

Trichostasis spinulosa is a common but often unnoticed skin condition involving bundled vellus hairs, especially in people with darker skin or UV exposure.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

CT60 polymorphism might increase the risk of Alopecia Areata.

Recent advances show zebrafish can model anemia, Alx4 affects craniofacial and hair development, and mTORC1 is crucial for retinal development.

Trichophyton mentagrophytes genotype VII is a sexually transmitted fungus causing skin issues, mainly among men who have sex with men in Europe, and requires quick treatment.

Topical and oral minoxidil are the best treatments for monilethrix.

Triamcinolone acetonide therapy for hair loss may cause a skin condition called linear lichen planus.

A new type of alopecia areata, called the "confetti variant," causes small bald spots that often heal on their own in a few months.

A rare form of alopecia causes hair thinning without bald spots and may be more common than thought, responding well to steroid treatment.

Recognizing perinevoid alopecia and concentric regrowth is important for diagnosing and treating alopecia areata.

Early recognition and treatment of scalp demodicosis can prevent misdiagnosis and effectively resolve symptoms.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Parthenolide promotes hair growth in mice and may influence pathways related to male pattern baldness.

Multiple trichofolliculomas can look like multiple trichoepitheliomas on the face.