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Basal cell carcinomas may differentiate similarly to hair follicles and could be influenced by hair cycle-related treatments.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Most patients with Central Centrifugal Cicatricial Alopecia at the reviewed institution were middle-aged Black women, often with no symptoms, and commonly treated with topical medications.

Hedgehog pathway inhibitors for advanced basal cell carcinoma can cause side effects, but managing them helps maintain treatment.

Patients with central centrifugal cicatricial alopecia may have a higher risk of breast and colorectal cancer.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

Blocking Hedgehog signaling offers new treatment options for advanced basal cell carcinoma.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Understanding and managing side effects of hedgehog pathway inhibitors can improve treatment for advanced basal cell carcinoma.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Hair follicle stem cell transplants can reverse liver cirrhosis by blocking harmful cell activation.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Tenofovir is more effective than adefovir for resistant hepatitis B, Fibroscan is good for assessing liver damage, regulatory T cells may help hepatitis C persist, and other insights into liver health and disease were found.

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

Elderly patients with CCCA were all African American with low vitamin D, but no iron or zinc deficiencies, and no hormonal imbalances compared to younger patients.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

Patients with central centrifugal cicatricial alopecia often have higher rates of metabolic, autoimmune, and atopic conditions, as well as anxiety and depression.

Older age is the main risk factor for hemorrhagic cystitis after stem cell transplants.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

The patient with both scarring and non-scarring hair loss showed complex immune reactions and improved with steroid treatment.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

Reflectance confocal microscopy reliably identifies skin cancer features like horizontal skin tissue sections.

CTHRC1 helps hair grow back, and plantar dermis mixture boosts it.

Early diagnosis with trichoscopy can improve management and quality of life for CCCA patients.