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Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

The congress showed that psychological therapy can help skin condition patients, social media affects acne stigma, education improves atopic dermatitis, and patient satisfaction in dermatology is high, especially with good doctor engagement.

Follistatin helps hair growth and cycling, while activin prevents it.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

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

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

Gene mutations can cause problems in male genital development.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

Skin changes throughout life, from development before birth to aging effects like wrinkles, influenced by both genetics and environment.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.

Facial dark spots can be caused by the sun, genetics, makeup, or medicine, and are diagnosed by patient history and skin tests.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Stem cell therapies show promise for treating various diseases but face challenges in clinical use and require better monitoring techniques.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

The conclusion is that different blood diseases cause specific oral symptoms and require varied treatments to manage these symptoms and improve patient health.

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

Half of people with Alopecia Areata may see hair regrowth within a year without treatment, but recovery is unpredictable.

Human skin makes sexual hormones that affect hair growth, skin health, and healing; too much can cause acne and hair loss, while treatments can manage these conditions.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

The conclusion is that proper signaling is crucial for hair growth and development, and errors can lead to cancer or hair loss.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

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

Some growth factors, while important for normal body functions, can cause diseases when not regulated properly.