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Taking L-tryptophan supplements might cause a condition similar to scleroderma in some people, which can get better after stopping the supplement and starting corticosteroid therapy.

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

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.

Two siblings have a rare hair condition caused by a new genetic variant.

Clouston Syndrome can be linked to rare sweat gland tumors.

Two siblings both had a rare case of alopecia areata at the same time.

A woman with anorexia developed gout from self-induced vomiting.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A patient with Cronkhite-Canada syndrome improved with nutritional support and steroids, but early diagnosis is key due to high mortality.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

A young woman with late-stage Vogt-Koyanagi-Harada disease was successfully treated at a hospital.

Neuromyotonia and morphoea can occur together in the same body areas.

Recurrent pneumothorax can occur in Sjogren's syndrome, even without common markers.

Thymoma may link myasthenia gravis, nail dystrophy, and alopecia areata.

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

Two babies needed surgery to remove hair tightly wrapped around their toes to prevent serious injury.

Alopecia areata is rare in organ transplant patients and may be linked to the drug tacrolimus.

Hair-tourniquet syndrome can cause serious toe injuries in infants but can be treated if found early.

A young woman with visual issues and other symptoms was diagnosed with lupus and antiphospholipid syndrome, and improved with treatment.

Anti-phospholipid antibodies in SLE can cause thrombosis and bone necrosis.

A Nigerian teenager was diagnosed with neuropsychiatric lupus, showing various severe symptoms and abnormal lab results.

Frontal Fibrosing Alopecia may be linked to autoimmune diseases like Sjögren's syndrome.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Patients with alopecia areata had higher TSH levels.

The patient with a misplaced pituitary gland and interrupted pituitary stalk is being treated with hormone replacement.

The conclusion is that skin, mucous, and eye problems after Stevens-Johnson syndrome and Lyell syndrome significantly affect patients' lives, highlighting the need for comprehensive care and eye check-ups.

A patient with Sézary syndrome showed improvement after treatment and the study suggested follicular mucinosis might indicate future lymphoma risk.

Levothyroxine treatment fully cured the young man's hypothyroid symptoms.