Search

everythinglearnresearchcommunity

for

Search:↓

New hair regrowth model proposed, imiquimod found to kill skin cancer cells, T-cadherin loss linked to invasive skin cancer, no clear gene link to skin cancer after transplant, and study on children's hair loss shows male dominance and genetic ties.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

Certain genes may promote longer root hairs in plants when phosphorus is low.

Cantú syndrome may be linked to pituitary adenomas.

Monilethrix is a rare genetic hair disorder with no cure, but low-dose oral minoxidil may help.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

The document discusses various skin disorders and new therapeutic approaches.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Asian hair loss differs from Europeans; consider individual needs and psychological well-being for treatment.

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.