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A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

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.

Most patients with hair loss sought treatment for cosmetic reasons, were unhappy about their appearance, and had a family history of the condition, suggesting it may be inherited.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

A single long white eyelash is a rare but benign condition.

Older, overweight women with children and a family history of hair loss are more likely to experience female pattern hair loss.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Nursing students in Turkey have a moderate acceptance of cosmetic surgery, influenced by education, urban background, personal connections to those who had surgery, perception of risk, and desire for awareness training.

The document concludes that pediatricians play a vital role in supporting adolescents through puberty and should enhance their competence in this area.

The document corrects a missing conflict of interest and acknowledges a pioneer in hair transplantation and his other contributions.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

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

Hormone levels in women with androgenetic alopecia are similar to those without the condition.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Implanted dermal papillae can induce hair growth in rat ear wounds.

Human hair and mouse whiskers emit similar biomagnetic fields.

The woman's hair loss was mainly due to stress and low iron levels, and her hair grew back after treatment.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

The research identified two types of keratinocytes in chicken scales: one for hard scales and another for soft skin, with similarities to human skin differentiation.

Hair growth can be induced by certain cells found at the base of hair follicles, and these cells may also influence hair development and regeneration.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

Minoxidil helps hair growth in people with monilethrix without side effects.

A 10-year-old boy had the earliest reported case of hair that became progressively kinkier but eventually returned to normal on its own.

Urologic diseases and treatments in older men can negatively affect fertility, and doctors should talk to patients about this.

Frequent hairdryer use may worsen hair fragility in people with Pili Annulati.

Men with moderate hair loss had the best spatial thinking, and long-term DHT might affect cognition.