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Epidermal nevi are skin cell clusters linked to various syndromes.

Accurate diagnosis and management of rare genian fistulas require combined clinical, radiologic, and histopathologic evaluations.

A young woman had a rare, usually non-cancerous tumor on her face that was initially mistaken for a different condition.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

A man with a birthmark on his scalp developed hair loss that improved with treatment, but the link between the birthmark and hair loss was unclear.

Dermoscopy is crucial for diagnosing rare scalp tumors like trichofolliculoma.

Fahr syndrome causes brain calcification and is managed by treating symptoms and underlying issues.

Most cases of high male hormone levels in women are due to polycystic ovary syndrome.

The tumor likely shows dual neural crest differentiation.

The study found unique skin changes in a rare type of alopecia linked to a skin condition called linear morphea.

Fibroblast changes in systemic sclerosis may help understand disease severity and treatment.

Hormones might affect the skin condition hidradenitis suppurativa, but their exact role is unclear.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Rapid virilization should be checked for possible ovarian or adrenal cancer.

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

Trichoscopy is a helpful tool for diagnosing Netherton syndrome.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

Three Iranian men had reddish-brown facial pigmentation with no effective treatment.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

Two patients with skin lupus were mistakenly thought to have a different scalp condition but improved with lupus treatment.

Mutations in keratin genes cause cell fragility and various skin disorders.

Rhupus is a complex syndrome that is hard to diagnose due to unclear clinical criteria.

Nevus sebaceous is identified by unique skin changes, including thickened skin, fewer hair follicles, and many sebaceous glands.

A young girl with high testosterone was thought to have a tumor but actually had PCOS, which was treated with birth control pills.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

The study concluded that severity of Frontal fibrosing alopecia is not linked to how long someone has it, can start before menopause, and eyebrow loss may be an early sign.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.