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Trichoscopy helps distinguish between scalp Discoid Lupus Erythematosus and Lichen Planopilaris for accurate diagnosis and treatment.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

The study concluded that a 'Swiss cheese' pattern in hair follicles is a useful sign for diagnosing alopecia areata.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

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

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

A unique type of lupus panniculitis causes reversible hair loss on the scalp in East Asians.

The study concluded that female pattern hair loss is linked to psychological distress and is hard to diagnose and treat, with its causes still not fully understood.

Schizophrenia risk genes may affect early brain development, contributing to the disease.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

Defective protein folding due to a mutation is key in ANE syndrome.

Two sisters had rare, widespread cysts and complete hair loss, suggesting a genetic link.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

A rare skin condition was identified and planned for treatment in an elderly man.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

Excessive vitamin A can cause symptoms that mimic serious brain conditions.

Trichoscopy is useful for diagnosing and monitoring systemic lupus erythematosus, with certain hair and scalp changes indicating more active disease.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Dermoscopy is useful for diagnosing lichen planopilaris and certain features may relate to disease duration, age, and gender.

Autophagy helps delay aging in mouse glands, maintains fat balance, and controls scent production.

The girl has a genetic hair condition causing thin hair since childhood.

Accurate diagnosis of SLE requires extensive testing due to its complex symptoms.

A 5-year-old boy has Nevus Comedonicus Syndrome, causing skin lesions and a cataract.

The patient had a severe itchy rash and hair loss in the armpits.

Dutasteride may help reduce brain plaque linked to Alzheimer's by affecting cell energy structures and waste removal.

The man likely has a condition causing eyelash loss and scaling on his eyelid.