Search

everythinglearnresearchcommunity

for

Search:↓

Teprotumumab for thyroid eye disease commonly causes fatigue, brittle nails, dry eyes, hair loss, muscle spasms, and dry mouth, with rare serious events like blood clots.

The tumor likely shows dual neural crest differentiation.

Promising treatments for EBS include anti-inflammatory drugs, antibiotics, creams, mTOR inhibitors, and gene editing, but more trials are needed.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

Cathepsin L is essential for normal hair growth and development.

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

A girl's hair loss was found to be caused by both a hair-pulling disorder and another hair loss condition.

Erlotinib can cause hair loss as a side effect.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Matriptase is crucial for skin barrier, hair growth, and may contribute to skin cancer.

A rare ear cyst contained hair fragments.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Congenital triangular alopecia can occur outside the typical fronto-temporal region.

Trichoscopy is a helpful tool for diagnosing Netherton syndrome.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Surgeons should know about pilomatricoma for accurate diagnosis, even though it's rare.

The boy had trichotillomania, causing hair loss, and treatment focused on habit reversal and support.

Selumetinib effectively reduces tumor size in many children with neurofibromatosis type 1, but can cause skin and hair issues.

Molluscum contagiosum can occur in epidermoid cysts, especially with prolonged steroid use.

Anti-Ku-positive patients often have muscle weakness and autophagy plays a key role in their condition.

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

Tofacitinib helped an 8-year-old child recover from a type of hair loss that is hard to treat.

CD19-CAR T cell therapy may help regenerate skin in systemic sclerosis.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

Tofacitinib improved arthritis and partially improved hair loss in a lupus patient without side effects.