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Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

The conclusion is that accurately identifying the cause of high androgen levels in women with PCOS is crucial and requires specific tests.

The conclusion is that formalizing how past decisions influence current health technology assessments could improve the credibility and defense of coverage decisions.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

Pioglitazone usually doesn't effectively treat or cure lichen planopilaris.

Pregnancy can cause specific skin conditions that need correct diagnosis and treatment to protect both mother and baby.

The document explains how to identify different hair problems using a microscope.

Type I interferons play a key role in the development of various skin diseases.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Early adrenal gland maturation in young children can be normal, but other serious conditions should be ruled out first.

People with Seasonal Affective Disorder have different brain activity in certain areas when resting.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Oral zinc sulphate reduces dark hair color in mice.

Amenorrhea is when a woman doesn't have periods, with primary amenorrhea starting by age 15 or within five years of breast development, and secondary amenorrhea when periods stop for three months. It affects 3-4% of women not pregnant, breastfeeding, or in menopause, mainly due to polycystic ovary syndrome, hypothalamic amenorrhea, hyperprolactinemia, and ovarian failure.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Immune cells help regulate hair growth, and better understanding this can improve hair loss treatments.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

ΔNp63α stops TAp73β from working in skin cancer by blocking its access to specific genes, not by directly interacting with it.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

New melanoma treatments can cause skin side effects, including skin cancer and rashes, but combining treatments may reduce these risks.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Methotrexate effectively treated a 2-year-old's generalized pustular psoriasis without side effects.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

Bimatoprost can cause longer, thicker, darker eyelashes and eyebrows.