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Lichen planopilaris and frontal fibrosing alopecia are likely the same disease with different clinical appearances.

Frontal fibrosing alopecia causes hair loss at the front hairline, and no effective treatment exists.

Intralesional corticosteroids and 5-alpha-reductase inhibitors are the best treatments for frontal fibrosing alopecia.

A reliable system was developed to distinguish hair growth stages, aiding in identifying hair growth promoters or inhibitors.

EGF controls hair growth by regulating hair follicles' growth phases.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

The control system for hair growth cycles is not well understood and needs more research.

RU 58841 may treat acne, hair loss, and excessive hair growth.

Rhino mice show significant meibomian gland changes, making them a potential model for studying gland disorders.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

Activating β-catenin in certain skin cells speeds up hair growth in mice.

Early stage bald spots are linked to skin inflammation and damage to the upper part of the hair follicle.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

HNG helps hair grow by keeping hair in the growth phase longer.

Stem cells from umbilical cord blood may prevent hair loss caused by certain medications.

Basal cell epithelioma-like changes are most similar to normal basal cells.

A girl with Netherton syndrome was able to eat wheat without allergies after a special treatment.

A new method can detect mutations in mice by observing changes in hair follicle cells.

Postmenopausal women may experience frontal hairline and eyebrow loss due to cicatricial fibrosis.

The neighborhood face index (NFI) accurately predicts properties of complex molecules.

Genetic markers can help predict ear shapes for forensic use.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Werner's syndrome causes early aging and increases cancer risk, requiring early diagnosis and symptom management.

Apoptosis is important in the hair cycle of dogs.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Human hair follicles can be grown in a lab for about a week.

Current treatments for postmenopausal frontal fibrosing alopecia stop hair loss but don't regrow hair.