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Intralesional cidofovir might be a viable alternative treatment for certain conditions.

A woman with severe hypothyroidism had a rare skin condition usually linked to a different thyroid disease.

High chromogranin A levels are linked to obesity and inflammation in polycystic ovary syndrome.

A 47-year-old man's eyelid swelling didn't improve with basic treatments, so a biopsy was needed.

PAON shows skin patterns due to genetic mosaicism.

Vogt–Koyanagi–Harada disease can cause rare hair growth on normally hairless thumb skin.

Follicular vitiligo causes hair to gray without skin color loss.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

The thyroid nodule was benign, and surgery was successful with a smooth recovery.

A woman was the first known case to have both polycystic ovary syndrome and autoimmune polyglandular syndrome type 2, suggesting a need to check for both conditions in similar patients.

A woman's rare scalp condition worsened after using a specific arthritis medication, suggesting such medications can sometimes trigger or aggravate psoriasis.

Most patients with dermatomyositis had skin rash and were treated with prednisolone and hydroxychloroquine.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

Cyclophosphamide often causes gastrointestinal issues, hair loss, and low blood cell counts in Chinese patients with autoimmune diseases.

Eosinophilic pustular folliculitis should be considered in teens with persistent skin issues for accurate diagnosis and treatment.

Tofacitinib significantly improved hair loss and lesions in a patient with overlapping autoimmune disorders.

Early diagnosis and targeted anti-inflammatory treatments can improve outcomes in androgenetic alopecia with perifollicular inflammation and fibrosis.

Pustules in toxic erythema are linked to hair follicles or sweat ducts.

A man with a rare disease experienced late hair whitening and loss, but hair color returned, suggesting a good outlook.

Tofacitinib significantly improved symptoms in a patient with overlapping autoimmune disorders.

Lacrimal gland inflammation and alopecia areata can happen together due to autoimmune issues.

Treatment improved some symptoms but not all.

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

Early recognition and management of gastrointestinal tuberculosis in lupus patients are crucial to prevent complications.

The role of γδT-cells in causing alopecia areata remains unclear.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

A gluten-free diet significantly improves skin and health issues in people with dermatitis herpetiformis, a skin condition linked to celiac disease.

A rare autoimmune condition, Satoyoshi syndrome, can start in adults and improve with immunosuppressive treatment.

Oral feline interferon-omega improved symptoms in diabetic cats with gingivostomatitis.