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Aggressive treatment in young patients with certain drug reactions may lead to multiple autoimmune diseases later.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

A woman with systemic sclerosis developed a unique scarring hair loss combining features of systemic sclerosis and frontal fibrosing alopecia.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

A woman with non-classic CAH had unusual heavy periods and high hormone levels, improved with treatment.

Hairy elbows may be linked to short stature, but the exact cause is unclear.

Consider Sertoli-Leydig cell tumors in Peutz-Jeghers syndrome patients with adnexal masses.

The woman's facial symptoms are best explained by primary Sjögren’s Syndrome.

A specific gene mutation causes Olmsted syndrome.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

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

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

A patient with zinc depletion improved after zinc supplementation during parenteral nutrition.

The four patients have a unique type of ichthyosis affecting hair follicles.

Satoyoshi syndrome is likely an autoimmune disease.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

A girl with a rare skin condition improved after one month of treatment with acitretin.

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

Routine genetic testing is crucial for early diagnosis and better management of Turner’s syndrome with 21-hydroxylase deficiency.

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

Infliximab can cause SAPHO syndrome, which may improve with Spesolimab and methotrexate.

Ketoconazole improved symptoms of ACTH-independent Cushing syndrome despite inconclusive initial scans.

Stopping steroids and providing supportive care improved the patient's Cushing Syndrome symptoms and ulcers.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

Early treatment with corticosteroids improved her eye condition significantly.

A 2-year-old girl had a hair disorder not shared by her identical twin.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.