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The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Key genes linked to hair growth and cancer were identified in hairless mice.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

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

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

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Ovulation disorders are a major cause of infertility and menstrual problems in women.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

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.

ACBP is essential for healthy skin and fur by maintaining the skin's barrier function.

Hair changes can indicate systemic diseases or medication effects.

Androgens can both increase body hair and cause scalp hair loss.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

The document explains the genetic causes and characteristics of inherited hair disorders.