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Anti-epileptic drugs may cause visual and hair side effects due to enzyme inhibition, especially in genetically predisposed individuals.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

COVID-19 vaccination may trigger recurrence of cutaneous T-cell lymphoma in some patients.

Abnormal T-cells from thymomas cause non-motor symptoms in some myasthenia gravis patients.

Visual field defects in lupus nephritis can be caused by hypertensive retinopathy, not glaucoma or medication toxicity.

TH antibodies in vitiligo and AA patients recognize the same protein parts.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

Vorasidenib can cause unusual hair growth.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Leukokoria can signal Coats disease or other retinal issues, requiring early detection to prevent severe outcomes.

A woman's rare hair loss condition improved on its own, suggesting this type might recover like common cases.

A woman's severe male-like symptoms were caused by a rare, benign tumor in her ovary that produced male hormones.

The report suggests that hair loss in Cronkhite-Canada syndrome may be caused by alopecia areata incognita, as shown by a patient's improvement with treatment.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Alopecia areata is becoming more common in Japan, with a need for better treatments, especially for severe and pediatric cases.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

Paraproteinemic keratopathy can show eye symptoms before other signs of disease, needing careful treatment and long-term follow-up.

Cyclooxygenase-2 overexpression in mice skin causes hair loss like human androgenetic alopecia.

Cyclosporine can cause a unique skin condition called "cyclosporine-induced folliculodystrophy."

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

The four patients have a unique type of ichthyosis affecting hair follicles.

Chronic granulomatous disease may be linked to developing systemic lupus erythematosus.

A JAK1 variant causes hair loss, skin issues, and thyroid disease, but treatment with a specific inhibitor can help.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

A rare type of skin cancer with mucosal involvement was partially treated but eventually relapsed.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

Lichen planopilaris can occur with multiple autoimmune diseases.