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Lithium therapy may cause skin problems like hidradenitis suppurativa and other side effects, which can improve after stopping the medication.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

SLHA can be hard to diagnose and needs teamwork between specialists.

Too much vitamin A can cause liver damage and skin issues.

Individualized assessment and meticulous planning are crucial for successful brow and upper eyelid surgery.

Hair highlighting can cause serious scalp burns if not done carefully.

A kidney transplant patient developed leprosy, likely due to immunosuppression and genetic factors, and improved with treatment.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Sarcoidosis can cause scarring hair loss on the scalp, which is rare.

A 10-year-old boy had the earliest reported case of hair that became progressively kinkier but eventually returned to normal on its own.

A man lost all his hair permanently after hepatitis C treatment, a side effect not seen before.

A rare autoimmune condition, Satoyoshi syndrome, can start in adults and improve with immunosuppressive treatment.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A tick bite caused temporary hair loss in a man, which is a rare condition that usually gets better within 3 months.

Gefitinib can cause hair and eyebrow darkening.

Gabapentin may cause hair loss in patients treated for neuropathic pain.

The method effectively reduces and hides scalp defects after surgery.

A rare pigmented skin tumor called melanotrichoblastoma was diagnosed in a 51-year-old woman.

The Indian Journal of Plastic Surgery has achieved a Journal Impact Factor of 0.8 and improved its Scopus CiteScore to 1.4.

Cashmere goats have a hair growth cycle with specific genes regulating growth, regression, and resting periods.

A man got heart infection from scalp infection caused by artificial hair implants.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

A rare skin tumor with extra hair growth was found and safely removed from a 27-year-old woman.

Upadacitinib may effectively treat twenty-nail dystrophy without causing pain.

Plica neuropathica can occur with diffuse alopecia and should be considered in diagnosis.

A woman with a rare hair loss condition developed skin cancer in the bald area.

An AI device for skin cancer was successfully integrated into the NHS, improving diagnosis accuracy and service capacity.

FAPD in children may not depend on androgens and should be treated with anti-inflammatory measures and minoxidil.

A 4-year-old had a rare type of hair loss that may have a good outcome.

Massive minoxidil ingestion can cause prolonged shock requiring extended supportive care.