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The study aims to find the best treatment for central serous chorioretinopathy by comparing various options.

Escitalopram helped a woman with hair-pulling due to long COVID.

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.

Misdiagnosis of hair and scalp disorders is common in patients with skin of color, highlighting the need for better training and evaluation.

Unique fat cells near fibrotic areas contribute to systemic sclerosis progression.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

Some medications for inflammation can cause a condition with scalp rashes and hair loss, often linked to Crohn's disease, and may require treatment changes to prevent permanent hair loss.

The study found that imaging might miss small ovarian tumors causing high testosterone, and suggested using certain testosterone levels and treatment responses to identify these tumors.

Surgeons should know about pilomatricoma for accurate diagnosis, even though it's rare.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

The woman had a genetic condition causing high cortisol and androgen levels, treatable with dexamethasone.

Trichilemmal carcinoma is rare, usually benign after removal, but needs close follow-up due to recurrence risks.

A 10-year-old girl's symptoms improved after surgery to remove a benign adrenal tumor.

Rare seminoma found in a 33-year-old woman with atypical genitalia and no Y chromosome.

Older patients with Cushing's syndrome often have different symptoms and treatment outcomes compared to younger patients.

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

A potential link exists between unexplained hormone deficiency, hair loss, and testicular tumors, suggesting thorough screening is needed.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Borderline newborn screening results should be carefully evaluated to prevent delayed diagnosis of thyroid issues.

Trichoblastoma in the breast can be mistaken for cancer, so expert review is crucial to avoid misdiagnosis.

A young girl had a rare neck cyst removed and needs careful monitoring for related health issues.

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

Temporal triangular alopecia usually starts in early childhood and treatment with Minoxidil has limited effectiveness.

A woman's Cushing's syndrome caused by adrenal cancer improved after surgery.

Acitretin effectively prevented skin cancer in a patient with late-onset Rothmund-Thomson syndrome.

Transgender men on testosterone therapy need ongoing gynecologic care due to potential cancer risks.

Group behavior therapy reduces hair-pulling symptoms more than supportive therapy but has limited long-term effectiveness.

A child with Sweet syndrome was found to have chronic granulomatous disease and improved with treatment.

Patients with metabolic syndrome had lower Gleason scores when diagnosed with prostate cancer.

New technologies show potential for better understanding and treating skin conditions with abnormal mucin, but more research is needed for clinical use.