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Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

A specific gene change in APCDD1 increases the risk of hair loss.

Skin problems are common in Bangladesh due to arsenic, prompt treatment of diabetic foot ulcers is crucial, maternal transmission causes most neonatal herpes, treatments for pediatric vasculitis are effective, the chickenpox vaccine works, more frequent UVB therapy helps psoriasis, certain jobs increase hand dermatitis risk, monoclonal antibodies treat psoriasis well, lifestyle affects psoriasis, alefacept improves psoriasis, imiquimod cream partially clears basal cell carcinoma, and iron may not help chronic hair loss.

Steroids, infection management, and nutritional support can significantly improve symptoms of Cronkhite-Canada Syndrome.

A man lost all his hair permanently after hepatitis C treatment, a side effect not seen before.

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

Poor nutrition is linked to increased hair loss in Canadian children.

Polycystic Ovary Syndrome (PCOS) is not very common among Iranian women, but it's important to prevent it because of the risk of heart disease and infertility.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

Patients on long-term hemodialysis often have skin problems related to their treatment.

Chemotherapy with docetaxel and cisplatin can cause severe low potassium, requiring careful monitoring and treatment.

Lichen planus pigmentosus may indicate undetected hepatitis C infection.

The study concluded that key signs of Keratosis follicularis spinulosa decalvans are changes in terminal hair and vellus hair follicles, which likely start the inflammation and damage to hair follicles.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Vitamin D protects skin cells from damage caused by captopril.

Diagnose and manage CCCA with thorough history, exams, and labs; treat with anti-inflammatory agents, stress reduction, and stopping harmful hair practices.

A 14-year-old boy was diagnosed with a rare hair condition that may lead to hair thinning and has no known effective treatments.

Primary care doctors need to monitor JAK and TYK-2 inhibitors carefully for skin conditions.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

CCCA is a common scarring hair loss in African descent women, possibly linked to genetics, hair care practices, and health issues like diabetes.

Graft-versus-host disease is a complication where donor immune cells attack the recipient's body, often affecting the skin, liver, and gastrointestinal tract.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

Increasing zinc intake improved skin and hair symptoms in a rare genetic disorder.

Scalp involvement in primary cutaneous lymphomas is common and can be aggressive, requiring careful attention.

Korean patients with PCOS often have skin problems like acne and excess hair, with different symptoms based on their specific PCOS type.