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The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

The document explains how to identify different hair problems using a microscope.

People with Alopecia Areata often have thyroid problems like Hashimoto thyroiditis and hypothyroidism.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The pandemic likely caused delays in skin cancer assessments, leading to fewer early diagnoses and thicker melanomas.

Matriptase is highly active in hair follicles and sebaceous glands, especially during hair growth phases.

People with atopic dermatitis are more likely to develop other skin conditions due to shared genetics and immune pathways.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Thyroid hormones affect skin texture, hair and nail growth, and can cause skin diseases related to thyroid problems.

The document recommends three dermatology books for their valuable content on evidence-based medicine, comprehensive treatment descriptions, and updated information on hair and scalp disorders.

Mimicking growth factors in a topical solution can prolong hair growth phase and reduce hair loss without side effects.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Nilotinib can cause keratosis pilaris, a skin condition.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Found new possible treatments for hair loss.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

Researchers created a skin graft that senses blood glucose and could treat diabetes using CRISPR-edited stem cells.

The most common skin condition at the Baqai Institute in Karachi was scabies, and eczema was the most prevalent group of diseases.

Cyclosporine cleared a woman's resistant skin condition quickly and kept it away for over a year.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

Minoxidil, tretinoin, and finasteride may help hair regrowth in mild to moderate androgenetic alopecia.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.