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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

ODC transgenic mice can model human hair loss with skin lesions.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

A man developed a rare skin condition and drug-induced lupus, highlighting the need for biopsy in diagnosing skin issues caused by sunlight.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

High-dose methotrexate can cause severe skin and nail issues.

Two cases of hairy elbows syndrome were described, with normal skin texture and symmetrical hair growth.

Melasma is a skin condition linked to female hormones, genetics, UV exposure, and certain medications, but not to pituitary, adrenal, or thyroid diseases.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

TBX3 gene affects horse coat color, with higher expression in darker areas.

A woman's severe skin reaction was caused by an allergy to a skin treatment.

Erosive pustular dermatosis of the scalp causes painful, scarring skin lesions on the scalp, mainly in elderly people with sun-damaged skin.

A new mouse mutation causes skin and hair defects due to a gene change.

The study found specific skin and cell changes in patients with monkeypox, helping diagnose and understand the disease.

A rare scalp condition was successfully treated with specific medications after 9 months.

A pregnant woman's skin condition improved after giving birth, possibly due to high estrogen levels during pregnancy.

Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Immunological skin diseases in pigs are rare and can be caused by immune system issues or external factors.

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

HLD10 can include increased body hair and Mongolian spots.

The patient was diagnosed with oral lichen sclerosus and needs long-term monitoring.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

EGFR-targeted cancer therapy can cause skin issues starting at hair follicles, leading to inflammation.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Vellus hair cysts can cause acne-like bumps that don't respond to treatment.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

A new gene mutation is linked to monilethrix in the studied family.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.