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Mutations in the LIPH gene cause woolly hair in a child.

Recognizing trichoscopic features is crucial for diagnosing various hair loss conditions.

A 9-year-old girl with a healthy immune system was successfully treated for a severe fungal scalp infection caused by Microsporum audouinii.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Researchers found a white halo around hair in most patients with a specific type of hair loss, which helps in early diagnosis and treatment.

The treatment improved hair color in most vitiligo patients without major side effects.

Children with chronic kidney disease often have skin, hair, and nail problems.

CDK inhibitors may help treat ARDS and psoriasis but need more testing for safety and effectiveness.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

Acitretin treats severe skin conditions but requires careful monitoring due to serious side effects.

Ritlecitinib is a new treatment for severe hair loss in people 12 and older.

24-Hydroxycholesterol reduces DHT formation in brain cancer cells, linking cholesterol and hormone metabolism.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Some patients with severe alopecia areata developed skin darkening from their treatment, which may indicate a less effective response to the therapy.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

Retinoic acid affects hair growth and can cause hair loss.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

Adalimumab helped control a child's severe eye disease when other treatments failed.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Retinoids can help treat skin disorders by improving the skin's outer layer.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

Vitamin B12 deficiency can cause reversible skin darkening.

Using dermoscopy improves diagnosis of scalp and hair disorders in children.

New treatments using stem cells and special materials show promise for severe eye surface disease.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

Patients with this syndrome can have different responses and worsening resistance to treatment over time.