Search

everythinglearnresearchcommunity

for

Search:↓

A gene mutation causes woolly hair in a Syrian patient.

Hair loss in women can be slowed with treatment, but more research needed for better solutions.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

The document concludes that recent studies help tell apart desmoplastic trichoepitheliomas from other skin tumors, but more research is needed for clear differentiation.

The conclusion is that PCOS is a common cause of hirsutism in young obese women, and early treatment is important to reduce the risk of metabolic syndrome.

Different types of atopic dermatitis were linked to specific genetic and immune changes, suggesting that severe cases might need stronger immune-targeting treatments.

Female pattern hair loss shows similar characteristics in both genders and should be classified by hair loss patterns, not gender.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Better models and evaluation methods for alopecia areata are needed.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

Genes controlling hair growth and immune response are disrupted in male pattern baldness.

The EDAR gene greatly affects hair thickness in Asian populations.

Different types of hair loss have unique features under a microscope, but a doctor's exam is important for accurate diagnosis.

Adult female acne requires a comprehensive treatment approach, including medical options and lifestyle changes, with attention to psychological well-being.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

Rare adrenal cancers that secrete androgens or estrogens have a poor prognosis and are treated primarily with surgery.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.

Women with PCOS and higher BMI, especially those with morbid obesity, are at greater risk for depression.

The document concludes that diagnosing and managing plaque psoriasis, particularly in sensitive areas, is challenging and requires careful differentiation from similar skin conditions.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

Minoxidil improved hair growth in a child with a rare genetic disorder.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.