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The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Chemotherapy may cause recurring hair loss due to an autoimmune response.

Inflammation and fibrosis are not significantly different in pattern hair loss compared to controls.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Tranilast successfully treated a man's skin sarcoidosis when other treatments failed.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Ritlecitinib shows promise as a versatile treatment for various autoimmune and inflammatory diseases.

Ovariectomized mice mimic postmenopausal hair loss, and estradiol helps maintain hair density.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Researchers developed a new method to quickly prepare skin cells that improve wound healing in rats.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Hair loss in a woman with eosinophilia-myalgia syndrome improved after stopping L-tryptophan and starting treatment.

The photographic method for measuring facial hair density is reliable and valid but needs further testing on different hair densities and skin colors.

A patient grew extra hair on their ears after treatment for testicular cancer, possibly due to hormonal changes or genetics.

The document concludes that Follicular Unit Hair Transplantation is a more precise and effective method for hair restoration.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Platelet-rich plasma is considered safe but needs more research to prove its effectiveness in medical treatments.

A 35-year-old man had patchy hair loss that was actually due to syphilis, not alopecia areata.

A woman experienced hair loss after taking strontium ranelate for osteoporosis.

The patient's long-term hair loss was caused by leukemia treatments and low estrogen levels, worsened by her genetic tendency for hair loss.

New instruments were introduced to make hair transplantation surgery more precise and improve graft survival.

Elastic Net DNA methylation clocks are inaccurate for predicting age and health status; a "noise barometer" may better indicate aging and disease.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Baldness and shaved heads change how traits are seen but don't really affect leader preferences.

Heptaminol may cause hair lightening in hemodialysis patients.

Drinking kava tea can cause a skin reaction with red, swollen bumps, which may improve with steroids.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

Clinicians should use social and prescription data to track trends in performance-enhancing drug use.

Topical minoxidil helped an 8-year-old boy with a genetic hair disorder grow hair.