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Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

Denosumab, a bone loss treatment, may cause hair loss and skin reactions due to immune system effects.

Finasteride treats hair loss but may affect prostate cancer detection.

Two patients with skin lupus were mistakenly thought to have a different scalp condition but improved with lupus treatment.

Men with a family history of hair loss are more likely to experience it themselves, especially if both parents have hair loss.

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

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Frontal fibrosing alopecia can occur in children, not just postmenopausal women.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Over half of young people in Saudi Arabia experience early gray hair, linked to factors like smoking, stress, and family history.

Taking 1 mg of finasteride daily could potentially treat rare hair conditions like Acquired Progressive Kinking of the Hair and whisker hair.

Sex and sex hormones can affect brain inflammation in Parkinson's disease, with male mice being more affected and female mice showing a protective effect.

The document suggests a possible link between mast cells and scarring alopecia, recommending more research for potential treatments.

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.

Vitamin D supplements may reduce hair-pulling in people with Trichotillomania.

Elkonyxis, a rare nail condition, improved when patients stopped their nail-picking habits.

No link found between aromatase gene and female hair loss.

Higher doses of isotretinoin may lead to more hair loss.

Oxidative stress contributes to hair graying and loss as we age.

The current understanding of frontal fibrosing alopecia involves immune, genetic, hormonal factors, and possibly environmental triggers, but more research is needed for effective treatments.

A male patient developed frontal fibrosing alopecia after antiandrogen therapy for prostate cancer.

A woman with lupus had muscle weakness due to kidney issues and was successfully treated with medication.

Paternal drug exposure can harm fertility, pregnancy outcomes, and offspring health, with specific drugs linked to various reproductive issues.

Combining minoxidil with MS injections leads to better hair regrowth in men.

Managing multiple autoimmune diseases in one patient is very challenging.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

A 5-year-old boy was diagnosed with congenital triangular alopecia, a type of hair loss without skin changes, usually starting between ages 2-5, with no specific treatment.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Dr. Shoji Okuda's early hair transplantation techniques were rediscovered after being overlooked due to World War II.