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A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

O'Tar T. Norwood was a key figure in creating a system to classify male baldness and founding hair restoration societies.

Rabbit hair fibers are similar to wool and have a hollow center like feathers.

Adult offspring of sperm donation generally feel positive about their conception and view the donor as their biological father.

Corneous beta-proteins evolved uniquely in reptiles and birds, forming scales, claws, beaks, and feathers.

Some skin medications can harm male fertility, but they don't seem to cause birth defects from father's exposure.

William Harvey is recognized for discovering blood circulation and pioneering experimental medicine.

New genetic mutations causing hair loss were found in a Chinese family.

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

A girl had rickets due to a gene mutation affecting vitamin D response.

Eruptive vellus hair cysts can run in families.

Dr. Shoji Okuda was a pioneer in hair transplant surgery, but his work was initially overlooked and is now recognized alongside Dr. Norman Orentreich.

The boy had a fungal scalp infection called kerion, which was cured with oral antifungal medication.

Albert Kligman, known for his dermatology research and the discovery of tretinoin, was a significant figure in hair science but faced controversy for inmate experiments.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

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.

The document corrects a name misspelling, acknowledges a pioneer in hair transplantation, and notes a missing conflict of interest disclosure.

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

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.

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

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

Biotin may help women with hair loss who have low biotin levels, but more research is needed.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.