Search

everythinglearnresearchcommunity

for

Search:↓

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The patient was diagnosed with oral lichen sclerosus and needs long-term monitoring.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Botulinum Neurotoxin-A can treat acne, oily skin, rosacea, hair loss, prevent scars, relieve nerve pain, reduce excessive sweating, and manage psoriasis, but more trials are needed to confirm its effectiveness.

A 15-year-old girl has a benign skin tumor on her neck.

Cornification is how skin cells die to form the protective outer layer of skin, hair, and nails.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

Cannabinoids may help treat various skin conditions.

New genetic discoveries may lead to better treatments for alopecia areata.

Primary cicatricial alopecia, a rare disorder causing permanent hair loss, is hard to diagnose and treat, with treatments like anti-inflammatory drugs and steroids offering varied results and no guaranteed cure. Psychological support for patients is important, and future research should aim to identify causes of the condition.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

iPSCs can help treat genetic skin disorders by creating healthy skin cells from a small biopsy.

A specific gene mutation causes Olmsted syndrome.

Eruptive vellus hair cysts are rare and often misdiagnosed, requiring biopsy for accurate diagnosis.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Certain natural and synthetic compounds may help treat inflammatory skin diseases by targeting a specific signaling pathway.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

The research found genes that change during cashmere goat hair growth and could help determine the best time to harvest cashmere.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

New genetic mutations linked to rare skin disorders were found in three newborns.

Retinoids are effective for various skin conditions and hair loss but have serious side effects, so low doses are recommended.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

The document explains breast development, common breast conditions, and their treatments.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

The document suggests a new way to categorize skin and mind disorders into two main groups to reduce confusion.

A patient with a scalp condition and benign skin tumor experienced hair loss and did not improve with treatment, choosing not to have surgery despite a small cancer risk.