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Asian patients with Frontal Fibrosing Alopecia often lose eyebrow hair and respond well to combined antiandrogen or antimalarial and topical treatments.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Topical minoxidil improves hair loss in 80% of women with breast cancer undergoing endocrine therapy.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

Mutation in hairless gene may increase hair loss risk.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Human hair protein modifications could potentially indicate heart disease risk.

t-Flavanone helps improve male pattern hair loss by making hair roots stronger.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Acitretin helped improve hand mobility and skin condition in a patient.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Using special RNA to target a mutant gene fixed hair problems in mice.

Different hair loss types need accurate diagnosis for proper treatment.

Hyperadrenocorticism in ferrets is linked to neutering and indoor housing, and is best treated with surgery and a deslorelin implant.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Iron deficiency might contribute to hair loss in women.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.