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The woman's skin and hair symptoms were confirmed as frontal fibrosing alopecia, and while facial papules are common in such cases, there's no effective local treatment, but systemic treatments can help.

A new gene mutation causes a rare type of hair loss.

Frontal fibrosing alopecia is a challenging hair loss condition with no known cause or definitive treatment.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

PPAR alpha may help in hair growth and could be a target for treatment.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

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

Lipin-1 is important for skin cell differentiation and skin barrier function.

Upper eyelid hyperpigmentation can help diagnose facial lichen planus pigmentosus in patients with frontal fibrosing alopecia.

Genetically at-risk healthy people show similar immune issues as those with Pemphigus vulgaris or Alopecia areata.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Linear lichen planopilaris can affect the trunk, not just the face.

sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

Pseudopelade is likely an independent disease due to its distinct features.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

The condition is likely inherited in an autosomal-dominant pattern.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Loose anagen hair syndrome may be caused by keratin gene mutations.

FFA's causes may include environmental triggers and genetic factors.

A child's rare skin disease was triggered by chickenpox.

Lipase H is important for hair follicle function and shaping hair fibers.

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

Hair follicle cells help protect against immune attacks by regulating T-cell activity.

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.