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Daily use of antifungal shampoo can hide symptoms and make it hard to diagnose fungal scalp infections.

A woman had a rare, non-cancerous skin growth on her face, which was removed and did not come back after a year.

Alopecia areata often starts around age 23, can be permanent in 30% of cases, and treatments are usually temporary.

PAD is common but often missed, needing lifestyle changes and medication for better outcomes.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

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

Frontal fibrosing alopecia may affect nails and could be a type of lichen planus, treatable with certain medications.

A 12-year-old boy's rare skin condition improved with topical treatments and may resolve by puberty.

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

Eruptive vellus hair cysts are rare and often misdiagnosed, requiring biopsy for accurate diagnosis.

Dermoscopy can non-invasively detect eruptive vellus hair cysts on the labia majora.

Traumatic anserine folliculosis is a skin condition caused by friction, treatable with topical cream and avoiding trauma.

Primary idiopathic pseudopelade of Brocq causes gradual, scarring hair loss with no effective treatment.

A 79-year-old man was diagnosed with a rare skin condition called nevus comedonicus on his eyelids.

Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

Relatives of women with PCOS symptoms are more likely to have similar health issues.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

The study concluded that careful examination is key to differentiate between lipidized fibrous histiocytoma and juvenile xanthogranuloma.

Eruptive vellus hair cysts are often missed in diagnoses.

Primary essential CVG is a rare, benign scalp condition with treatment focusing on symptom management and hygiene.

Paraproteinemic keratopathy can show eye symptoms before other signs of disease, needing careful treatment and long-term follow-up.

The conclusion is that surgical removal of solitary fibrofolliculoma is effective with no relapses, and diagnosis requires a biopsy due to varied symptoms.

A man with a skin nodule was diagnosed with a rare skin condition called cutaneous focal mucinosis, which can be confused with other skin cancers.

A rare skin condition affected only the facial hair of a 46-year-old man.

Consider TFI in facial hypopigmentation diagnoses and confirm with a biopsy.

Dermoscopes help tell FPHL apart from other hair loss types and can detect it early by identifying specific patterns.

Integrating ABI screening in clinics can improve patient care for those at risk of peripheral artery disease.