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Newborns with the common rash Erythema Toxicum have many active mast cells in their skin, but these cells don't produce the LL-37 peptide.

Pigmented rings with central clearing help diagnose melasma more accurately.

A rare case showed basal cell carcinoma and leiomyosarcoma coexisting, needing careful diagnosis and treatment.

New treatments for chronic central serous chorioretinopathy show promise in preventing permanent vision loss.

Kerion is a severe scalp infection that needs quick treatment to avoid permanent hair loss in children.

The lemur's testicular tumor was removed, improving its coat and behavior, with no signs of cancer spread.

PRP injections for hair growth can cause temporary vision loss, which may be resolved with treatment.

Orbital decompression surgery for Graves' orbitopathy caused double vision in 19% of patients, with similar rates for two surgical methods.

Connexin mutations can cause various diseases like hearing loss and skin disorders.

Keloids on the penis are rare, often triggered by circumcision, and rarely recur after surgery.

Early diagnosis and teamwork are crucial for managing ILVASC effectively.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

The condition is harmless, doesn't worsen, and needs no invasive treatment.

Most people with basal cell carcinoma on their head or neck were 60-70 years old, and it often came back even after being fully removed, especially in certain areas and types.

Immunohistochemistry helps accurately identify and differentiate malignant trichilemmoma.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Consider Sertoli-Leydig cell tumors in Peutz-Jeghers syndrome patients with adnexal masses.

Peripheral nerve blocks are a safe and effective way to treat various headaches and provide lasting pain relief.

Eyelid pilomatrixomas are rare, benign tumors that need accurate diagnosis for proper treatment.

Tangent screens help detect visual field defects from vigabatrin.

The boy had severe facial swelling and scalp infection after using his mother's shampoo.

A gene mutation in mice causes skin defects and early death.

Recognizing IPPP is crucial to prevent misdiagnosis and unnecessary treatments.

Hair-shaft abnormalities can indicate neurological disorders, some of which are treatable.

Limbal Mesenchymal Stem Cell Secretome might help heal eye injuries by reducing inflammation and promoting tissue repair.