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A 21-year-old with lichen planopilaris was successfully treated, stopping disease progression and preventing crusts.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

Correct diagnosis is crucial for treating overlapping conditions like NMOSD and SLE effectively.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Early diagnosis and comprehensive management improve life quality for Netherton syndrome patients.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

An 11-year-old obese girl was diagnosed with lipedematous scalp, a condition with swollen scalp tissue usually found in adult women.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

A 16-year-old girl with a hair-eating disorder needed surgery to remove a hairball from her stomach and small bowel.

Researchers identified a new hair loss pattern called "sisaipho type," where hair is lost across the scalp except around the edges.

Ganser syndrome may result from both organic and psychogenic factors.

A woman in Sri Lanka was diagnosed with lupus after presenting with protein loss from the gut and other symptoms.

Wearing a wig caused a woman's skin condition to worsen due to pressure from the wig's fasteners.

A rare skin condition with cysts was found on a 5-year-old boy's scalp.

Pilomatricomas are often linked to genetic syndromes, especially Apert syndrome, and genetic analysis is crucial for diagnosis.

A rare scalp condition can occur due to leukemia affecting the skin.

A woman with lupus had muscle weakness due to kidney issues and was successfully treated with medication.

Ulcerative sarcoidosis in body folds is rare and improved with prednisone and hydroxychloroquine.

Long eyelashes in a patient were an unusual sign of systemic lupus erythematosus.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

Recognizing the "bamboo hair defect" is crucial for diagnosing Netherton's syndrome.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

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

Lupus panniculitis of the scalp causes linear hair loss and needs ongoing treatment to prevent recurrence and lupus.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

A neglected leprosy treatment led to rare scalp hair loss in an Indian woman, which improved with proper medication.

A patient with a rare form of lupus improved after treatment for skin ulcers and hair loss on the face and scalp.

Consider Werner syndrome in young patients with early aging signs and metabolic issues.

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