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Obesity worsens PCOS symptoms, and PCOS may lead to more weight gain; managing both requires a holistic approach that includes mental health.

Male pattern baldness involves hormones and cell signals affecting hair growth.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Lymphocytes, especially CD8+ T cells, play a key role in causing alopecia areata, and targeting them may lead to new treatments.

Genetic variations affecting skin structure play a key role in severe acne.

Some families have a genetic condition where they are born with irregular scalp defects.

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

Genetic marker rs12558842 strongly linked to male hair loss.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.

A young man with an unusual type of scarring hair loss suggests a possible new variant of a known scalp condition.

Women with androgenetic alopecia have fewer terminal hairs, phenol in nail surgery is safe, and a new hair transplant method is faster and less damaging.

The study found that family history, personal history of adolescent acne, no pregnancies, hirsutism, office work, stress, and low intake of fruits/vegetables and fish are risk factors for adult female acne.

2011 dermatological research found new skin aging markers, hair loss causes, skin defense mechanisms, and potential for new treatments.

Early and aggressive treatment of scarring alopecia is important to prevent further hair follicle damage.

Ifidancitinib, a JAK inhibitor, effectively regrows hair in mice with alopecia by tiring out harmful T cells.

ILC1-like cells can independently cause alopecia areata by affecting hair follicles.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Some small molecule antivirals show promise against COVID-19, but more research is needed to understand and improve them.

People with hair loss conditions may also have thyroid disorders, but more research is needed to understand the connection.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Genetic discoveries are leading to new treatments for alopecia areata.

New topical treatment using spherical nucleic acids shows promise in reducing psoriasis inflammation.

Different connective tissue disorders have unique symptoms and treatments, with varying outcomes and often require ongoing care from a specialist.

Patients with severe alopecia areata have higher levels of MIF, which decrease after successful treatment.