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Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Equine Cushing's disease in horses causes hormonal imbalance, leading to symptoms like abnormal hair growth and requires lifelong treatment with pergolide.

The guideline refines PCOS diagnosis, promotes a healthy lifestyle, reviews treatments, and stresses long-term follow-up.

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

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

The document provides a quiz for physicians to earn continuing medical education credits in facial plastic surgery.

Black women with CCCA are more likely to have uterine fibroids.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

Cognitive behavioral strategies help women with PCOS make lifestyle changes to improve their health.

Men with CCCA often face delayed diagnosis and severe hair loss, highlighting the need for earlier recognition and treatment.

Dermatoscopy can help diagnose CCCA without visible hair loss, offering a less invasive option than biopsy.

PPAR-γ helps control skin oil glands and inflammation, and its disruption can cause hair loss diseases.

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.

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

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

Hair loss in African American women, caused by hair care, genetics, and environment, needs more research for better treatment.

WomenCare helps predict PCOD risk in women to encourage early medical consultation.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

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

ATP-sensitive potassium channels are important for hair growth.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

AP collagen peptides help hair grow and improve hair health.

Traditional Chinese medicine may help relieve symptoms of Cronkhite-Canada syndrome.