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The new AI software predicts melanoma outcomes more accurately than traditional methods.

Follicular red dots can appear where alopecia areata and vitiligo overlap.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

Human skin can make serotonin and melatonin, which help protect and maintain it.

Alopecia areata involves immune system changes, especially in severe cases, with potential new treatment targets identified.

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

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Key genes influence melanin in chicken muscles, affecting their value.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Lasers can help reduce skin side effects from cancer treatment.

Acitretin effectively prevented skin cancer in a patient with late-onset Rothmund-Thomson syndrome.

Shiny white structures in trichoscopy can indicate long-standing discoid lupus erythematosus alopecia.

Avoiding allergens can improve skin and hair conditions in adults with allergic reactions.

Treating melasma in men is difficult, especially for the deeper skin layers, and may need more than just topical treatments.

New genetic mutations causing hair loss were found in a Chinese family.

Early regulatory T cells are crucial for normal skin pigmentation.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Gene sequencing is essential for diagnosing junctional epidermolysis bullosa.

A rare case of scleredema in a diabetic woman showed loss of sweat glands, causing heat strokes, with treatment only slightly improving symptoms.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Most lupus patients in coastal Kerala had skin-specific lesions that could help diagnose the disease, and non-specific skin issues were linked to more severe, systemic lupus.

Shrinking skin cancer increases the chance of cancer in nearby lymph nodes.

New treatments and understanding of skin lupus are emerging in 2024.

Ponatinib can cause a rare skin reaction that resolves with topical treatment and temporary drug discontinuation.

A young Caucasian girl had both woolly hair and alopecia areata, which is rare.