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Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

DHT reduces a cell's ability to promote hair growth, while 3D culture without DHT improves it.

The endocannabinoid system affects oil production and inflammation in skin cells.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

A specific mutation in PA-PLA1α causes abnormal hair growth.

Certain fats in the skin help control inflammation and health, and changing these fats through diet or supplements might treat skin inflammation.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

FGF5 gene mutations cause long hair in domestic cats.

Alopecia Areata is an autoimmune condition often starting before age 20, with varied treatment success and a need for personalized treatment plans.

The review says skin conditions with sterile pustules need more research for better treatments.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The document concludes that changes in eyelashes and eyelid skin can indicate various local and systemic diseases.

The document concludes that skin and nail changes can indicate various underlying health conditions.

Colchicine might help treat different skin diseases, but more research is needed to confirm its effectiveness and safe dosage.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Postmenopausal hyperandrogenism, a condition with symptoms like increased hair growth and acne, is usually caused by PCOS but can also be due to other factors. It's diagnosed by checking testosterone levels and treated either by removing the adrenal tumor or through antiandrogen therapy.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Hair growth dysfunction involves various conditions with limited treatment options.

Acrodermatitis enteropathica is a rare inherited disorder causing skin issues, diarrhea, and hair loss.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

The document explains the diagnosis and characteristics of woolly hair nevus and alopecia neoplastica.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.