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Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Blocking the Hedgehog pathway may help overcome drug resistance in multiple myeloma.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The study concluded that careful examination is key to differentiate between lipidized fibrous histiocytoma and juvenile xanthogranuloma.

Topical patidegib gel effectively treats basal cell carcinoma in Gorlin syndrome patients without causing the side effects seen with oral treatments.

A man's rare tumor caused unusual nerve-related symptoms that improved after surgery.

A 16-year-old girl with lupus symptoms improved with treatment despite negative ANA tests.

Skin problems are common after stem cell transplants, and early treatment by dermatologists can improve patient outcomes.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

A new gene mutation is linked to monilethrix in the studied family.

Dermoscopy can help assess the severity of chronic radiation-induced skin damage in head and neck cancer patients.

The hairless gene mutation causes baldness by disrupting hair follicle structure.

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

Early diagnosis and treatment of Kaposi varicelliform eruption are crucial to prevent severe complications.

A rare skin condition appeared on a 19-year-old woman's scalp.

Early diagnosis and treatment of hereditary vitamin D-resistant rickets (HVDRR) are crucial to prevent growth issues and other health problems.

A patient with a rare chromosome condition also had a rare type of hair loss.

Scalp melanomas are more dangerous and likely to recur or cause death than other head and neck melanomas.

Aggressive treatment in young patients with certain drug reactions may lead to multiple autoimmune diseases later.

A 3-year-old boy had a rare hairball condition usually seen in teenage girls.

Children with HIV often have skin problems that can indicate the severity of their immune system damage.

Trichodysplasia spinulosa is a rare skin condition caused by a virus, treatable with antiviral medication.

Timely and aggressive treatment is crucial for improving outcomes in severe complications of adult-onset Still's disease.

The child was diagnosed with cutaneous leishmaniasis.

The research found that chickenpox virus spreads in skin through blood then to skin cells, while shingles virus moves from nerves to hair follicle areas before infecting skin cells.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.