Search

everythinglearnresearchcommunity

for

Search:↓

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Indigofera tinctoria leaf extract has many compounds that support its traditional medicinal uses.

A girl with Netherton syndrome was able to eat wheat without allergies after a special treatment.

Chocolate has been historically used for medicinal purposes, with current research focusing on heart health benefits, but the extent of these benefits is debated.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Some acne medications have side effects; doctors should educate patients and may not need to do frequent lab tests for all.

SGK3 is essential for proper hair growth and health.

Adult stem cells with Tp63 can form hair and skin cells when placed in new skin, showing they have hidden abilities for skin repair.

Using 5% topical minoxidil improved and normalized the hair growth in a girl with short anagen hair naevus.

Key genes can rewire networks, changing skin appendage types.

CD61 is important for mouse tooth cell growth and works through Lgr5.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

Hyaluronic acid filler can safely and effectively improve facial contour in Parry-Romberg Syndrome.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

A woman with acromegaly experienced severe hair loss from a drug called Lanreotide Autogel, which improved after stopping the treatment.

A woman with high testosterone and an adrenal nodule had an ovarian tumor causing her symptoms, which improved after the tumor was removed.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Hair loss can be a key sign of a rare type of rickets when vitamin D treatment doesn't work and advanced tests aren't available.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Using minoxidil and tretinoin on the skin, along with oral vitamin D, improved hair thickness and density in two girls with woolly hair.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Human hair structure varies by ethnicity, and certain treatments can improve hair condition and appearance.

Onions may help reduce cancer risk and obesity-related issues.