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The malignant pilomatricoma showed strong epithelial keratin expression, suggesting it may not calcify.

The Apc gene is crucial for normal skin and thymus development.

Knuckle darkening can be an early sign of vitamin B12 deficiency.

Seborrheic keratosis is a common, harmless skin growth that can look like cancer, so it may need a biopsy.

A boy's hair turned red because of genetic mutations, not lack of zinc.

BMP signaling controls hair growth and skin color.

Follicular vitiligo causes hair to gray without skin color loss.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

A man with both skin lesions and lung cancer improved quickly with chemotherapy, suggesting the skin condition might be a reaction to immune system injury.

Taiwan reported its first case of a rare scalp condition with no clear cause or treatment.

Certain VDR gene changes can affect melanoma risk.

Type XVII collagen helps control skin cell growth and may have anti-aging effects.

New mutations in the DSG4 gene cause a rare hair condition.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

A missing mK6irs1 gene causes hair loss in mice.

An 80-year-old woman with Cronkhite-Canada syndrome had multiple polyps and symptoms like diarrhea, hair loss, nail issues, and dark skin.

Melanin granules can be expelled by exocytosis.

The hr gene is linked to hair loss in Valle del Belice sheep.

Early diagnosis and prednisone treatment can improve outcomes in Cronkhite-Canada syndrome.

Brown skin in guinea pigs has more ascorbic acid and related enzymes, black skin uses ascorbic acid well, and white skin has the most protein.

Cows in El-Behera have nutritional deficiencies causing health issues like anemia and poor reproduction.

NGAL indicates abnormal skin cell differentiation.

Goats' hair and color traits are linked to specific RNA expressions, useful for breeding and textiles.

A rare lupus case in Bangladesh improved with specific treatment.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

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

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

Ectopic acanthosis nigricans can occur at surgical sites due to skin graft mismatches.