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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

HAIRCARECUBE TM (HCC) helps hair products work better by getting active ingredients deeper into the hair.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

Alcohol dependence affects stress hormone levels more than childhood maltreatment.

SCD1 is important for hair growth by keeping the connection in skin cells where hair stem cells live stable.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

WS Biotin, a new form of D-Biotin, improves water solubility and shows potential for hair and skin care without being toxic at low levels.

In alopecia areata, certain immune cells increase and express a protein linked to immune activation.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

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

Ultrasound can help detect early signs and severity of hidradenitis suppurativa.

Frequent blood transfusions in beta thalassemia patients can lead to thyroid problems.

Secukinumab reduces immune activity in hidradenitis suppurativa skin.

The model helps understand scar contraction and develop new treatments.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Two cases of hairy elbows syndrome were described, with normal skin texture and symmetrical hair growth.

BIVV009 is a safe treatment for bullous pemphigoid that reduces C3 deposition without harmful side effects.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.

Different tumor cells in one basal cell carcinoma can cause mixed treatment responses, suggesting personalized treatment is needed.

Human hair follicles can be used to create heart muscle cells.

An infant had two different natural hair colors on the scalp with no health issues.