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A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Hair loss in men can be slowed or reversed with treatments like minoxidil and finasteride, but it resumes if treatment stops. It may also indicate early heart disease and obesity.

Early recognition and treatment of tinea capitis are crucial to prevent severe scalp issues and prolonged therapy.

Children with cancer had slightly more unusual facial shapes than healthy kids, but not enough to easily tell them apart.

VEGF helps squamous cell carcinoma grow in ways beyond just blood vessel formation.

Troglitazone increases subcutaneous fat in lipodystrophy patients.

Docetaxel often causes hair loss, with limited effective treatments and no cure for permanent hair loss.

Androgenic alopecia causes hair thinning, and treatments include minoxidil, finasteride, and light therapy.

The C3H/HeJ mouse model is useful for studying and testing treatments for alopecia areata.

Germinated hemp seed extracts help prevent hair loss and promote hair growth.

Current treatments for androgenetic alopecia manage symptoms but don't cure it, and it affects social and psychological well-being.

Recent selection on immune response genes was identified across seven ethnicities.

Honeybees face serious threats from various diseases, but beekeepers use several methods to manage and control them.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Different androgen concentrations affect wool-related gene expression differently in Hetian and Karakul sheep breeds.

A rare scalp condition, cutis verticis gyrata, was found in a woman with primary scarring alopecia.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

Targeted cancer therapies can cause skin side effects, but activating SOS in the skin may help reduce them.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Alopecia areata in children is more common in boys, mainly affects the scalp, and is linked to genetics and psoriasis.

A girl's hair-pulling condition improved greatly after she started vitamin D treatment.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

The supplement highlighted advancements and challenges in plastic and reconstructive surgery, including the impact of smoking, chemotherapy, and new treatments like Tafluprost for hair loss.

Cicatricial alopecia, a permanent hair loss condition, is mainly caused by damage to specific hair follicle stem cells and abnormal immune responses, with gene regulator PPAR-y and lipid metabolism disorders playing significant roles.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

A patient with a rare chromosome condition also had a rare type of hair loss.

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

The document concludes that early diagnosis and treatment of PCOS in teenagers is important for managing symptoms and preventing long-term health problems.