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Selumetinib causes skin and hair side effects in kids with NF1, affecting treatment and quality of life.

Younger patients with severe alopecia areata often have nail problems.

Mitochondriopathy may cause eyelash loss.

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

People with hypothyroidism and hair loss often have more hair and scalp issues than those without thyroid problems.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

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

Zinc treatment improved skin and hair issues in a boy with a zinc-related condition.

VEGF-A is crucial for normal skin function and may be linked to psoriasis.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Keratin patterns in hair follicles help understand hair growth and potential hair and nail disorders.

A chimeric keratin partially improved skin structure in mice lacking keratin 5, but didn't fully restore normal skin.

Melasma's causes include genetics, sun exposure, hormones, and oxidative stress, and understanding these can help create better treatments.

Skin acetyl-CoA synthesis is crucial for overall lipid balance.

Natural products may help treat skin inflammation from abnormal adrenal hormones.

Addressing biological changes in lipids, metabolism, and microbiota may help treat hair loss in young Chinese females with oily scalps.

Children with alopecia areata should only have thyroid screening if they have Down syndrome, a history of atopy, family history of thyroid disease, or signs of thyroid problems.

Goats with BSE or scrapie show varying symptoms, and using only clinical signs may not detect all scrapie cases.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Topical immunotherapy can treat alopecia areata, but its effectiveness varies and the exact mechanism is unclear.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

Alopecia areata patients, especially women with nail issues or atopic diseases, are at higher risk for other autoimmune diseases.

Some recovered COVID-19 patients experience skin, hair, and nail issues, suggesting they need follow-up care.

Gefitinib can cause hair and eyebrow darkening.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.

Losing both ERBB2 and ERBB3 receptors in mice causes significant skin problems and inflammation.

Immune cells might contribute to hair loss caused by a specific mutation.