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PRP injection for hair growth can cause reversible vision loss due to inflammatory optic neuropathy.

Surgical excision is an effective treatment for persistent nodules from poly-L-lactic acid injections.

Different tumor cells in one basal cell carcinoma can cause mixed treatment responses, suggesting personalized treatment is needed.

A man had rare skin tumors with bone formation and cholesterol deposits.

The patient had paraneoplastic pemphigus without mucosal involvement.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

A man developed a skin cancer called folliculotropic mycosis fungoides after a kidney transplant.

Folliculotropic Mycosis Fungoides requires stage-based treatment, with early stages using skin therapies and advanced stages needing aggressive treatments.

VKHD and sarcoidosis may share a common cause.

The man has a disease causing skin patches, thickened nerves, and mild muscle weakness.

Targeting the HEDGEHOG-GLI1 pathway could help treat keloids.

A woman's large nose growth was initially misdiagnosed, but later confirmed to be giant rhinophyma after full removal and examination.

The study concluded that scalp tumors show different patterns based on age, gender, and tumor thickness, and emphasized the importance of early detection and scalp examinations.

Long-standing benign tumors can become cancerous, especially in people with weakened immune systems.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

An 86-year-old man had a rare tongue melanoma but refused treatment, showing the need for early cancer detection and treatment.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

A transwoman developed a brain tumor after nine years of hormone therapy, suggesting a possible link between the treatment and tumor development.

A woman's masculine features were caused by a rare ovarian tumor that produced male hormones.

Untreated congenital adrenal hyperplasia can lead to complications like stroke and needs glucocorticoid treatment.

A man had a rare stroke possibly due to taking finasteride, which might have increased his hormone levels causing a blood clot. His memory loss didn't fully recover even after stopping the medication.

The patient's hair had unique damage and a lower sulfur-to-nitrogen ratio compared to relatives, but not compared to healthy controls.

A 9-year-old girl developed type 1 diabetes and alopecia after being treated for a rare kidney disease.

Basal cell carcinomas in mice can start from hair follicle stem cells and other skin cell types, depending on signaling levels.

The flap advancement technique effectively treats severe scalp skin conditions, preserving hair and improving appearance.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

DMBT1 and galectin-3 may help suppress epithelial skin cancer.

A Rathke's cleft cyst caused hormonal imbalances and symptoms in a 68-year-old woman.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.