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Women with PCOS may have a higher risk of Alzheimer's disease.

Diphenylcyclopropenone (DPCP) effectively treated both alopecia areata and verruca vulgaris.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Mutations in keratin genes cause cell fragility and various skin disorders.

People with blood group O may have a higher risk of developing post-COVID-19 syndrome.

Three genes linked to the development of trichilemmal cysts were found.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Idiopathic hypoparathyroidism is rare and can be managed with dihydrotachysterol.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Monilethrix Syndrome causes fragile, beaded hair that breaks easily and needs early diagnosis for better care.

AS-OCT is crucial for diagnosing VZV interstitial keratitis and avoiding unnecessary treatments.

Rapid virilization should be checked for possible ovarian or adrenal cancer.

Pygo2 is important for early growth and progression of intestinal tumors, and could be a target for treating cancers with certain mutations.

An HIV patient with IRIS had rare syphilis symptoms affecting skin, eyes, and nerves.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

TICE salvage chemotherapy is effective for treating germ-cell tumors with poor prognosis.

Radiation therapy with chemotherapy can cause severe, long-lasting hair loss.

A rare scalp condition, cutis verticis gyrata, was found in a woman with primary scarring alopecia.

An 80-year-old patient grew new hair on a wound, showing that elderly people can still regenerate hair.

A doughnut-shaped wart can form after cryotherapy in people with alopecia areata due to immune system issues.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

La detección temprana y precisa de la pseudopelada de Brocq es crucial para detener su progresión.

A 15-year-old girl with rare reproductive disorders received hormone therapy to develop secondary sexual traits, but infertility persisted.