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A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Dilated scalp capillaries might be a sign of hair loss related to COVID-19.

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.

Steroid sulfatase inhibitors could help treat hormone-related disorders and cancers.

TSC2 is crucial for proper hair follicle development and patterning.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

People with chronic hair shedding have lower antioxidant levels in their blood compared to healthy individuals.

Testosterone boosts fluid and electrolyte secretion in seminal vesicles, aiding sperm function.

PROTAC technology shows promise for cancer treatment but needs more effective E3 ligase recruiters.

Interferon, especially alfa interferon, is an effective treatment for cutaneous T-cell lymphoma with manageable side effects.

A patient with Cronkhite-Canada syndrome improved with nutritional support and steroids, but early diagnosis is key due to high mortality.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Toe Tourniquet Syndrome is often misdiagnosed.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

The guidelines recommend informed consent for gender-affirming treatments and stress the importance of personalized, culturally sensitive care for transgender individuals.

Removing Ctip2 in skin cells causes skin inflammation similar to atopic dermatitis.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Cognitive-behavioral therapy with habit reversal training is the most effective treatment for trichotillomania.

Removing hair wrapped around the labia quickly prevents serious tissue damage.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Chronic Telogen Effluvium is a hair loss condition in middle-aged women that usually doesn't lead to complete baldness.

TLR2 is important for hair growth and can be targeted to treat hair loss.

A new method using 1,4-n-butylene dimaleate effectively repairs and strengthens damaged hair.

Different ligands change the shape of the TRPV3 ion channel in unique ways.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

Emotional stress can trigger intermittent hair loss in chronic telogen effluvium, which may not improve with treatment if stress continues.