Search

everythinglearnresearchcommunity

for

Search:↓

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Oral ciclosporin A and topical treatments both reduce hair loss and scaling in dogs with sebaceous adenitis, but using both together is most effective.

Five Weimaraners had a milder form of color dilution alopecia causing hair loss and skin issues.

Vitamin A might be a safe extra treatment for dogs with sebaceous adenitis, but more research is needed to prove its effectiveness.

A rabbit with sebaceous adenitis was effectively treated with ciclosporin and medium-chain triglycerides.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Erythromelanosis follicularis faciei can also affect women, though it's rare.

A 17-year-old in Saudi Arabia was diagnosed with a rare skin condition causing red-brown facial patches.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Woolly hair is a rare genetic condition with no effective treatments.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

A child with rickets and hair loss might have a rare type of rickets that doesn't improve much with usual vitamin D and calcium treatment.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Testosterone and dihydrotestosterone treatments can help with penile growth in males with 5α-reductase type 2 deficiency, with dihydrotestosterone being more effective in infancy.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Certain gene variations increase the risk of alopecia areata in Koreans.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Using steroids can increase the risk of heart problems.

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Researchers found two genes that may explain why some Casertana pigs don't have hair.