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A new treatment using a special gel with miR-665 reduces inflammation and helps hair regrow in alopecia areata.

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VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.

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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Mutations in the KRT16 gene can cause skin and nail disorders.

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

A new group called the Asian Association of Hair Restoration Surgeons (AAHRS) has been created.

A new therapy for a skin blistering condition has not been developed yet.

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Continued ritlecitinib treatment can lead to hair regrowth in some patients with alopecia areata who initially don't respond.

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A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

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A KRT32 gene variant causes loose anagen hair syndrome.

Certain gene variations are found in people with polycystic ovary syndrome.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

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