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Researchers found three types of melanocytes in developing mouse skin, each with different genes and locations.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

Reflectance confocal microscopy helped diagnose and manage a woman's hair loss without needing a biopsy.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

The newborn's skin blisters healed without scarring, leaving some light spots, and stopped forming after four months.

A 308 nm excimer laser successfully treated a boy with a rare skin condition after about a year of weekly sessions.

Hair transplantation can improve scars after removing a rare skin cancer.

Certain chemicals cause hair graying in black mice but not yellow mice.

Polarized microscopy helps identify hair irregularities in genetic disorders.

Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

Multiple perifollicular fibromas may actually be unrecognized cases of Birt-Hogg-Dubé syndrome.

A 14-year-old boy has a skin condition called nevus comedonicus, treated with tretinoin cream.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

An 8-year-old girl had a rare, benign skin tumor on her forehead.

Skin can produce blood cells, often due to disease, which might lead to new treatments for skin and blood conditions.

Skin changes help detect graft-versus-host reaction early after bone marrow transplants.

A woman had a unique skin growth with hair follicle, oil glands, fat cells, spindle cells, and nerve fibers.

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

Larger nail cavity sizes suggest benign tumors, while smaller ones may need further biopsy to rule out cancer.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

Melanocytes are crucial for skin pigmentation and can affect conditions like melanoma, vitiligo, and albinism, as well as hair color and hearing.

The nodule was a benign cutaneous lymphadenoma, not cancer, and was successfully removed.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Apoptosis in hair follicles spreads through cell death signals, with stem cells slowing the process.

The digital system for measuring melasma shows promise but needs more development for better accuracy and automation.

A new one-step test can quickly identify skin cancer during surgery.