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A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

Most skin changes during pregnancy are harmless and moles don't significantly change, but many women experience pigmentation changes due to hormones and sun exposure.

DMBT1 and galectin-3 may help suppress epithelial skin cancer.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

The ferret had a malignant apocrine gland tumor and did not survive surgery.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

A new molecule was found to be a safe and effective skin lightener and anti-aging product.

Adrenomyeloneuropathy (AMN) can cause bladder problems due to nerve damage.

Podiatrists need more training to detect foot melanoma early.

Annurca apple extract promotes hair growth by changing hair follicle metabolism to boost keratin production.

A 21-day-old baby had a skin rash that didn't improve with cream and wasn't caused by a fungus.

Uveal melanoma is hard to treat when it spreads, but a new drug, tebentafusp, helps patients live longer.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

Early recognition and treatment of atypical alopecia areata in infants are crucial.

Lichen planus pigmentosus mainly affects middle-aged women with darker skin, is underreported, and is hard to treat.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Leukemia can sometimes appear as unusual skin issues in children.

Oxygen levels affect hair growth and color cells differently when they interact directly.

The man has a disease causing skin patches, thickened nerves, and mild muscle weakness.

A 7-year-old girl with non-scarring alopecia will have hair follicle transplantation to improve her quality of life.

NGAL indicates abnormal skin cell differentiation.

Pilomatricomas don't follow the usual hair follicle cell differentiation process.

A 79-year-old man was diagnosed with a rare skin condition called nevus comedonicus on his eyelids.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.

Low oxygen levels improve the function of hair and skin cells when they are in direct contact.

Some cases of short anagen hair syndrome are linked to specific genetic variations that are also connected to male pattern baldness.