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Eating too many paradise nuts for cancer prevention caused a woman to lose all her hair due to selenium poisoning.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

Most patients with Tuberous sclerosis had neurological or skin issues, and over half had psychiatric problems.

A man with Klinefelter syndrome had a leg ulcer that didn't heal well, even with treatment.

Alopecia areata incognita causes widespread hair loss without patches and needs a scalp biopsy for diagnosis.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

Scientists turned mouse stem cells into skin cells that can grow into skin layers and structures.

Most Korean systemic lupus erythematosus patients experienced hair loss, often as non-scarring diffuse hair loss, with non-scarring patch alopecia also common.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

No treatment has been proven to effectively stop hair loss or regrow hair in Frontal Fibrosing Alopecia, and more research is needed.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Fungal infection was the main cause of hair loss in Egyptian children studied.

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

Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.

A patient lost all their hair while on rheumatoid arthritis medication.

If a child is losing a lot of eyelashes and it keeps happening, doctors should look carefully at their health history because it might be a sign of a different health problem.

A child's hair loss after Kawasaki disease may help understand the disease's autoimmune causes.

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

Human hair keratin can be used in many medical applications.

The report found a new type of hair loss in African-American women that affects more areas of the scalp than previously thought.

Treating hair loss in both men and women is effective and improves quality of life.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

The conference concluded with plans for joint research into children's skin conditions and emphasized the importance of collaboration and patient-focused research.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

The conclusion is that skin, mucous, and eye problems after Stevens-Johnson syndrome and Lyell syndrome significantly affect patients' lives, highlighting the need for comprehensive care and eye check-ups.

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

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.