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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.

Chronic scarring alopecia is common in SLE patients and needs early detection and management.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

A rare scalp condition, cutis verticis gyrata, was found in a woman with primary scarring alopecia.

Sarcoidosis can cause scarring hair loss on the scalp, which is rare.

Ayurvedic treatments can improve symptoms and quality of life for systemic sclerosis patients.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A woman with anorexia improved significantly after being treated for scurvy with vitamin C, despite not showing typical scurvy symptoms.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

Most spinal cord injury patients in Korea experience skin problems, especially fungal infections and eczema, affecting their quality of life.

An elderly man had a rare, large skin cyst on his lower back, which was removed by surgery.

Powered exoskeleton training improves body perception and quality of life in spinal cord injury patients.

Parry Romberg syndrome requires awareness and teamwork in primary care for proper diagnosis and management.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Early recognition and multidisciplinary management are crucial for improving outcomes in Parry-Romberg syndrome.

Early diagnosis and tailored treatment are crucial to prevent permanent hair loss and support self-esteem in children with scarring alopecia.

Pre-surgical embolization and a two-stage resection improve outcomes for rare sacral tumors.

Severe sarcoidosis often requires long-term systemic corticosteroids and multidisciplinary care, with most patients improving but some experiencing persistent symptoms or complications.

Early scar classification in lupus can improve treatment and patient outcomes.

Scurvy still occurs today and can be diagnosed by symptoms like gum bleeding and a specific rash, confirmed by low vitamin C levels.

Rare skin cancer can mimic hair loss conditions, so thorough diagnosis is crucial.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

Obesity and certain hormone levels can lead to advanced bone age in young girls with early breast development.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

A 21-year-old male has a rare scalp condition with excessive skin folds.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

Hair loss was likely caused by gymnastics activities on a balance beam.