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A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Understanding intermediate filaments helps explain hair health and related diseases.

A woman with Fox-Fordyce disease had symptom relief using tretinoin cream.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.

The study found that long-term sun exposure does not significantly affect follicular plugs on the scalp, and the scalp's appearance is unique compared to other body parts.

Tretinoin may be effective for treating Fox-Fordyce disease.

A new method was developed to extract and analyze proteins from very short human hairs.

Tiny infundibular cysts are the main lesions in chloracne, not comedones.

A 12-year-old boy's hair loss and skin issues improved significantly with medication.

Fine wool sheep have more genes for wool quality, while coarse wool sheep have more for skin and muscle traits.

The onychodermis helps anchor the nail bed and may aid in nail formation.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Monotreme hair structure and protein distribution are similar to other mammals, but their inner root sheath cornifies differently, suggesting a unique evolution from reptile skin.

Yellow dots in hair and scalp examinations are important for diagnosing different scalp conditions.

Dermoscopy helped diagnose discoid lupus erythematosus in two patients without needing skin biopsies.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

The study found clear differences in lesion distribution and microscopic features among trichostasis spinulosa, keratosis pilaris, and eruptive vellus hair cysts.

The document found differences in lesion distribution and microscopic features among trichostasis spinulosa and similar skin conditions.

Laminin 332 is essential for normal skin cell behavior and structure.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Lymphotoxin-β is crucial for proper skin development in embryos.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

Keratinocytes from dog hair follicles can create a functional skin layer in a lab model, useful for dog skin therapy.

Human hair cells can change based on their environment, especially interactions with certain skin cells.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

Trichostasis spinulosa is a rare skin condition with hair-filled plugs in hair follicles.

Intermediate filaments are crucial for cell differentiation and stem cell function.

HPV16-transformed cells can change human skin cell properties, aiding tumor growth.

Traumatic anserine folliculosis is a skin condition caused by friction, treatable with topical cream and avoiding trauma.