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AGA can occur in children with family history; early diagnosis and treatment important.

The document describes the signs of different common types of hair loss.

Five Weimaraners had a milder form of color dilution alopecia causing hair loss and skin issues.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

The 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

Some drugs can cause changes to your hair.

Some skin diseases and their treatments can negatively affect male fertility.

Early baldness in men may indicate risks for obesity, metabolic syndrome, insulin resistance, and heart disease, similar to women with PCOS. Alopecia areata is often linked with autoimmune diseases and mental health issues. Certain hair disorders are due to genetic issues, and chemotherapy can cause hair loss through specific biological pathways. Iron deficiency's link to hair loss is still disputed.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Hair transplant surgery effectively treated a specific type of hair loss and is recommended as a primary treatment option.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

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.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Benzoyl peroxide and adapalene gels work differently to reduce acne in mice.

Hair follicle stem cells in hairpoor mice are disrupted, causing hair loss.

The article suggests that hair transplant surgery may not be purely cosmetic because it treats a disease and calls for clearer guidelines on its classification.

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

Three dogs with a rare skin condition improved with treatment.

The document concludes that understanding and managing hair loss in cancer patients is important, and more research is needed for better treatments.

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.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Malnutrition can cause unusual eyelash growth and hair loss.

Researchers identified specific genes that are important for mouse skin cell development and healing.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.