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The study found that alopecia areata and hypothyroidism increase the risk of each other, but androgenetic alopecia and hypothyroidism do not.

Atopic dermatitis increases the risk of some autoimmune diseases.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

Patients with one autoimmune disease should be checked for other autoimmune disorders.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

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

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

Pregnancy can cause various skin changes and diseases, with PUPPP being the most common skin condition specific to pregnancy.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Oral zinc sulphate reduces dark hair color in mice.

Hair microscopy is useful for diagnosing certain hair loss conditions but has limitations and must be interpreted carefully.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Assessing newborn scalp hair can reveal important health information.

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.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Most hirsutism cases are due to PCOS, and treatment focuses on lowering testosterone and blocking its effects.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

NF-κB signaling is crucial in many diseases and can be targeted for new treatments.

Histone modification is key in treating chronic inflammatory skin diseases.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Acne is genetically linked to a higher risk of depression, anxiety, schizophrenia, and bipolar disorder, with the strongest link to bipolar disorder.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.