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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.

Father's finasteride use may affect son's fertility and testicular function.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

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.

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.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

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.

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