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Injecting a person's own fat stem cells into their skin can make it look younger and improve double eyelids for over a year.

Taking thyroid medication reduced the patient's pituitary gland swelling and improved her symptoms.

Forehead creases are formed by a tight connection between the skin and muscle through dense fibers, with changes in skin thickness and fewer skin appendages near the creases.

Perforating folliculitis is a skin condition with small bumps that may be linked to other diseases and is hard to treat.

The chemical peel improved the appearance of hand spots safely and effectively.

A painless cheek lump was misdiagnosed but found to be a rare, benign skin lesion called pilomatrixoma, treatable by surgery.

Liposomal carriers can improve tissue regeneration by stabilizing and retaining growth factors.

Erlotinib can cause unusual hair growth, like long eyelashes and facial hair.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

The patient's hair has unique structural differences with alternating bright and dark bands.

Acitretin improved monilethrix symptoms temporarily, but they returned after stopping treatment.

Women with acromegaly often have irregular periods due to hormone imbalances and growth hormone effects.

Skin can become dry and thick in hypothyroidism.

A 20-year-old woman had stable Progressive Hemifacial Atrophy and Vitiligo after treatment, suggesting a possible link between the conditions.

Monilethrix is not caused by a metabolic defect.

The document concludes that treatment improved skin lesions but not scalp hair loss in two patients with Graham-Little-Piccardi-Lassueur syndrome.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

RCM and dermoscopy help identify different types of hair loss in children.

Thyroid hormone and epidermal growth factor affect hair angle, tooth eruption, and ear development in rats.

A rare hair follicle disorder can cause itchy, bluish-black bumps on the body.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

The twins' condition is unique and doesn't match any known syndromes.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

Recognizing trichofolliculomas is important to avoid unnecessary surgery.

The LED device safely improves neck skin appearance without affecting thyroid function.

Facial trichostasis spinulosa is a chronic condition with significant cosmetic impact, especially in young women.