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A patient had both chronic lupus and systemic scleroderma, requiring careful treatment to manage symptoms.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

A Laotian man with unusual skin changes and multiple growths in his gut was diagnosed with Cronkhite-Canada Syndrome and improved with nutritional and immune-based treatments.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

Brow lifts raise and smooth the forehead and can lower the hairline.

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.

Pseudopelade is likely an independent disease due to its distinct features.

Latanoprost eye drops caused excessive cheek hair growth and eyelash whitening in a woman.

Frontal fibrosing alopecia can occur in children, not just postmenopausal women.

Gene sequencing is essential for diagnosing junctional epidermolysis bullosa.

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

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

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

A young girl developed unusually long eyelashes with a hair loss condition without other health issues or medication causes.

Cutaneous lupus erythematosus is a chronic skin disease that can progress to systemic lupus in some cases and requires treatment to prevent recurrences and scarring.

A man's forehead and eyebrow were successfully reconstructed with a skin and hair graft that matched his other eyebrow, without needing frequent trimming.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

A 61-year-old Filipino man had a skin condition that looked like another disease, making diagnosis difficult.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

A patient had both chronic cutaneous lupus erythematosus and frontal fibrosing alopecia.

A woman had a cyst in her salivary gland, likely from Botox, which was removed and confirmed as an epidermoid cyst.

Cosmetics and procedures can cause eye issues, from mild discomfort to serious conditions, due to allergies, toxins, or poor care.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.

A rare skin condition causes red and dark patches on the face and limbs.

Congenital atrichia is a rare condition where children are born without hair, and treatment is often ineffective.