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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A man with four autoimmune diseases suggests a new category for multiple autoimmune syndrome.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

A rare benign tumor was found in a man's scrotum, highlighting the need for accurate diagnosis.

Using cidofovir cream for a rare skin disease can cause skin darkening.

Total skin electron therapy is an effective treatment for mycosis fungoides, balancing effectiveness and side effects.

Giant keratoacanthoma can look like squamous cell carcinoma, requiring careful diagnosis and surgical removal.

A new syndrome may link skin, growth, mental, and hair issues.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

People with weakened immune systems, like those with SLE, are at higher risk for TB.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

Skin and mucous symptoms are key for diagnosing autoimmune connective tissue diseases.

Grafted human scalp samples on mice can produce human hair, useful for studying hair genetics.

Ultrasound effectively distinguishes trichilemmal cysts from epidermoid cysts.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Milia, SM, and EVHC may be related conditions, not separate ones.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Temporal triangular alopecia is a non-scarring hair loss seen in some Asian children.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

A girl with citrullinemia developed pili torti, suggesting a link between the hair condition and the metabolic disorder.

Trichilemmal cysts may form from hair follicle outer root sheath growth.

Keratoacanthoma is a common, usually non-dangerous skin tumor that looks like squamous cell carcinoma but rarely becomes severe.

Immunohistochemistry helps accurately identify and differentiate malignant trichilemmoma.

Overexpressing PKCepsilon in mice reduces papillomas but increases carcinomas.

A young woman with lupus developed tuberculosis due to weakened immunity from her medication, showing the need for better TB screening in such patients.

TYK2 inhibition may help treat alopecia areata by promoting hair growth and reducing immune response.

Inhibiting mTORC2 can reduce DNA repair and increase cancer cell death, suggesting potential for targeted brain cancer treatments.

Activated LEF/TCF complexes are crucial for hair development and cycling.

CTCF protein is essential for skin and hair follicle development in mice.