Search

everythinglearnresearchcommunity

for

Search:↓

A rare skin lesion in a 64-year-old woman was successfully treated with a laser, showing minimal redness and no return after one month.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Skin tags may be linked to metabolic syndrome.

An elderly man's non-healing scalp lesion was successfully treated with a strong topical steroid.

The Polish Dermatological Society recommends personalized treatment for cutaneous lupus, including lifestyle changes, medications, and monitoring, with specific drugs for severe cases.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Increasing isoleucine intake improved skin and health issues in an infant with maple syrup urine disease.

A woman's cyclic Cushing syndrome was caused by a tumor in her adrenal gland that produced ACTH.

MESTSV is a rare tumor that is mostly benign but needs long-term monitoring due to potential recurrence.

Tumid lupus erythematosus can cause non-scarring hair loss on the scalp and requires careful diagnosis.

Systemic lupus erythematosus is a complex autoimmune disease mainly affecting women, with varied symptoms and unknown exact cause.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

A patient had both chronic lupus and systemic scleroderma, requiring careful treatment to manage symptoms.

Cronkhite-Canada Syndrome often leads to death within 6-18 months.

Facial trichostasis spinulosa is a chronic condition with significant cosmetic impact, especially in young women.

Hormonal changes and social stress may link lupus and eating disorders in teens.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Popliteal Artery Entrapment Syndrome (PAES) is a rare but possible cause of leg pain during walking, even in untrained women.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Physical symptoms in depression can reveal underlying medical conditions.

Managing severe infections in SLE patients requires tailored treatment strategies.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Rapunzel syndrome is more common in Asian countries and requires early diagnosis, especially in Asian girls.

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

SJS/TEN survivors often have severe, overlooked long-term physical problems that are not properly treated after leaving the hospital.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

Chronic cutaneous lupus erythematosus should be considered when acne treatments don't work.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.