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Afro-textured hair needs personalized care due to its unique genetic traits.

Gynostemma pentaphyllum and its component damulin B could help hair grow by activating certain cell pathways.

TLR2 helps control hair growth and regeneration, and its reduction with age or obesity can impair hair growth.

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

The skin acts like an endocrine organ, producing hormones that affect various body functions and skin health, and understanding this can lead to new treatments.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Understanding how acne develops in different diseases could lead to new treatments.

Oxidative stress and immune dysfunction are linked to both Hashimoto's thyroiditis and polycystic ovary syndrome, with diet and specific treatments important for managing these conditions.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

The document lists various dermatology topics, treatments, and diagnostic methods.

Taking Propecia might lead to the development of cataracts.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between 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.

DHT, a testosterone byproduct, causes male pattern baldness.

Scarring alopecias are complex hair loss disorders that require early treatment to prevent permanent hair loss.

Lifestyle changes are the main treatment for PCOS, which is a complex condition requiring early management to reduce its health impacts.

The protein SLC1A3 is important for activating skin stem cells and is necessary for normal hair and skin growth in mice.

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

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

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

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

The document concludes that corticosteroids effectively treat vasculitis allergica in over 90% of cases, with long-term kidney issues being the main adverse outcome.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Understanding where cancer cells come from helps create better prevention and treatment methods.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.