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Early diagnosis and aggressive treatment are key for managing rare scalp disorders that cause permanent hair loss.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Increasing olanzapine caused hair loss in a woman, which stopped after changing medication.

Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

Skin symptoms can indicate endocrine disorders and have various treatments.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

The document concludes that pig iPSCs show promise for transplant therapies and the field is advancing in controlling cell behavior for biology and medicine.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

New genetic mutations linked to rare skin disorders were found in three newborns.

Six genetic conditions are often linked to complete scalp hair loss in children.

Long-term use of Risperidone may be linked to a serious skin condition in bipolar patients, affecting their overall well-being.

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

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Tissue environment greatly affects the unique epigenetic makeup of regulatory T cells, which could impact autoimmune disease treatment.

Some women with PCOS have rare genetic variants linked to the condition.

Androgenetic alopecia is a common hair loss condition influenced by various factors and linked to psychosocial and cardiovascular issues.

Blocking specific proteins can help remove aging cells and might treat age-related diseases and promote hair growth.

Some skin conditions, like psoriasis and early-onset baldness, may indicate metabolic syndrome, and others are linked to diabetes risk and cardiovascular issues.

Lindera aggregata has many beneficial compounds that can help prevent and manage diseases.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Osthole inhibits the TRPV3 channel by binding to specific sites, potentially aiding drug development for skin diseases and cancers.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Treg cell-based therapies might help treat hair loss from alopecia areata, but more research is needed to confirm safety and effectiveness.

Oral retinoids are effective for severe skin conditions but require careful use due to side effects.