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A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

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CCC1 is essential for pH balance and normal cell function in plants.

ILC1-like cells can cause alopecia areata by themselves.

PP2Acα is essential for proper hair and skin development.

The ALADIN score can predict how well patients with alopecia areata will respond to JAK inhibitor treatments.

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

TAGX-0003 protected hair follicles and reversed alopecia areata in a mouse model.

Higher levels of certain DNAs in blood may indicate hair follicle damage in alopecia areata patients.

Abrocitinib helped a 14-year-old girl with severe alopecia areata regrow her hair significantly.

Epigenetic changes in blood cells may contribute to alopecia areata.

A new one-step test can quickly identify skin cancer during surgery.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

Krtap11-1 is important for hair strength and structure.

The study identified key immune cell differences between mild and severe alopecia areata.

miR-5110 affects alpaca pigmentation by altering specific gene expressions.

New treatments for skin conditions show promise, especially Coacillium® for hair growth in young people with alopecia areata.

A new model uses specific blood markers to predict if children's hair loss will return.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Baricitinib was effective in treating hair loss in adults with alopecia areata according to patient feedback.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Patients with advanced breast cancer prioritize quality of life, overall survival, and progression-free survival in treatment decisions.

Alopecia areata involves immune system changes, especially in severe cases, with potential new treatment targets identified.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Cantú syndrome may be linked to pituitary adenomas.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Hair transplants can effectively treat hair loss from CCCA in African American women if there's no inflammation.