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The paper concludes that the 1982 criteria for diagnosing systemic lupus erythematosus need updating to improve accuracy and involve dermatologists in the process.

Temporal triangular alopecia is a lifelong condition with hairless patches on the side of the head that may be present from birth.

A woman with lupus had hair loss and skin issues that were successfully treated with medications.

Leflunomide and anthralin may effectively treat severe alopecia areata.

Correcting EDA fibronectin organization and YAP translocation can improve wound healing in fibrotic conditions.

The Juri Temporo-Parieto-Occipital Flap is a good option for scalp reconstruction and hairline restoration with a natural look, despite some risk of necrosis and scarring.

A woman's progressive hair loss was correctly diagnosed as a rare condition called fibrosing alopecia in a pattern distribution after initially being mistaken for a more common type.

The method allows for 3D tracking of hair follicle stem cells and shows they can regenerate hair for up to 180 days.

Retinoic acids temporarily change skin stem cells to a slower cycle and more differentiated state.

The technique effectively shows how human skin and hair cells form into ball-like structures.

PC-associated alopecia has unique microscopic features.

Newer midface lift techniques are safer, more reliable, and have quicker recovery times.

The human amniotic membrane is a promising material for skin treatments and hair growth.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

Most cases of Temporal Triangular Alopecia are found in early childhood and may be related to genetic conditions.

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

AGD1's PH domain is essential for its role in root hair growth and polarity.

Early diagnosis and strong corticosteroids are crucial for managing lymphocytic cicatricial alopecia.

Healing psoriatic plaques can cause unexpected hair growth.

These hair loss conditions might be part of a spectrum, not separate issues.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

The patient's hair has unique structural differences with alternating bright and dark bands.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

The horse had a rare type of hair loss caused by immune cells attacking hair follicles.

Surgical deactivation can significantly reduce or eliminate migraine symptoms.

CCCA and lichen planopilaris have similar histological features, making them hard to distinguish.