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Fat-derived stem cells show promise for treating skin issues and improving wound healing, but more research is needed to confirm the best way to use them.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

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

New treatments and diagnostic methods for various animal skin conditions showed promising results.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Taking too many vitamin and mineral supplements can cause serious health problems.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Hair loss can indicate or worsen with systemic diseases, and treating the underlying condition is important.

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

Iron deficiency might contribute to hair loss in women.

Understanding skin structure and development helps diagnose and treat skin disorders.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.