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SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

Marking nuts can cause skin irritation and allergies.

Hair casts can be treated with physical removal and special shampoos.

Facelift surgery has evolved to focus on natural results and safety, with patient selection and postoperative care being key to success.

Nevus psiloliparus lacks mature hair follicles but keeps other skin structures intact.

Kerion is a severe scalp infection that needs quick treatment to avoid permanent hair loss in children.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Trichostasis spinulosa can be diagnosed with a simple skin biopsy and treated with specific gels, but lesions may return after stopping treatment.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

Hair melanocytes help the skin respond to stress and regulate hair pigmentation.

The method quickly analyzes hair growth genes and shows that blocking Smo in skin cells stops hair growth.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

Ruxolitinib treatment may cause eyelash growth.

Besnoitiosis, a parasitic disease, has been found in donkeys in Italy and may be more common in Europe than previously thought.

Tryptanthrin effectively suppresses non-melanoma skin cancer and is safe for normal skin.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

New research suggests that skin cell renewal may not require a special type of cell previously thought to be essential.

Polymer dot nanozymes and exosomes, with laser stimulation, speed up wound healing.

Injecting newborn mice with a niacin blocker caused skin, gut, and brain damage similar to human pellagra.

A specific gene mutation causes Olmsted syndrome.

A calcified nodule on a boy's face came from hair follicles and expelled calcium through the skin.

Understanding how new hair follicles form after skin injury could help prevent scars.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

Stress can cause hair to turn gray by depleting stem cells.

Shaving and avoiding brushing improved the patient's beard hair condition.

Hair casts can be mistaken for lice, so correct identification is important.

Netherton syndrome in a boy caused skin and hair issues, and treatment didn't work.