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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.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

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.

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

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

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

The Yorkshire terrier has a genetic hair loss condition not improved by treatment.

Genes and hormones cause hair loss, with four genes contributing equally.

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.

Cantú syndrome may be linked to pituitary adenomas.

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.

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.

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 woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

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.

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.