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Alopecia areata patients have more Propionibacterium acnes and less Staphylococcus epidermidis on their scalps.

Sarcoidosis is more common and severe in Black patients than in Caucasians, requiring early diagnosis and treatment.

Treating H. pylori infection might help cure alopecia areata.

English springer spaniels are more prone to severe sebaceous adenitis than standard poodles.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Skin side effects from cancer treatments can lead to changes in therapy and are common, with nail changes being the most frequent.

A woman's skin darkened after using dutasteride and pimecrolimus for hair loss, but improved when she stopped the medications and protected her skin from light.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

Further research is needed to understand how the microbiome affects hair loss in Alopecia Areata.

Different causes of beard hair loss have various treatments, including medications, lifestyle changes, and procedures to stimulate hair growth.

In Poland, people search more for certain skin conditions depending on the season, and despite more STD infections, searches for them have decreased, suggesting a need for better sexual education.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Imiquimod can cause rare skin side effects, some irreversible, and long-term follow-up is important for users.

Six genetic conditions are often linked to complete scalp hair loss in children.

Zinc levels are not significantly linked to the presence or severity of alopecia areata.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

Prednisolone improved symptoms in a woman with Cronkhite-Canada syndrome, but regular screenings are needed due to cancer risk.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

Pregnancy can cause normal skin changes that usually go away after childbirth and don't need treatment.

Alopecia areata is an autoimmune hair loss condition treated with corticosteroids, and histologic confirmation is the best diagnosis method.

Alopecia areata is complex, often recurring, and needs personalized treatment, especially with other health issues.

Dupilumab helped improve skin and prevent new lesions in a child with a rare immune disorder and severe eczema.

Preventive measures and effective management are crucial for reducing skin side effects in cancer treatment.