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A family had a rare fungal infection called white piedra, identified as Trichosporon inkin.

Topical corticosteroid was not more effective than placebo for children's alopecia areata, and atopy did not change treatment results.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

Dermoscopy helps accurately diagnose temporal triangular alopecia, avoiding unnecessary treatments.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

Hair restoration techniques and new cell sources improve hair loss treatments.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Canadian porcupines in a Japanese zoo passed a skin fungus to each other.

Idiopathic hirsutism causes excessive hair growth in women, can be treated with medication and hair removal, but cannot be fully reversed.

The document concludes that diagnosing PCOS requires a thorough approach, considering various symptoms and risks, and calls for improved methods to identify PCOS types and prevent diabetes.

Isotretinoin can raise CPK levels, so patients need monitoring, especially before surgery.

Two siblings have a rare genetic condition causing curly, coarse hair.

The document likely offers guidance on treating a woman's excessive hair growth, considering her symptoms and obesity.

Blocking COX, especially COX-2, in the skin can reduce inflammation and pain and may help prevent skin cancer.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

The study found that horizontal sections of scalp biopsies are better for analyzing hair loss, showing fewer hairs and more fine hairs in balding areas.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Prostaglandin E2 affects human platelet activity in complex ways that could lead to personalized heart disease treatments.

Facial dark spots can be caused by the sun, genetics, makeup, or medicine, and are diagnosed by patient history and skin tests.