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The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

The study suggests hormonal factors may play a role in Frontal Fibrosing Alopecia and that treatments like oral antiandrogens and steroids could be beneficial.

Gender-specific analysis could improve treatment for childhood systemic lupus erythematosus.

Skin, hair, and nail changes can help detect eating disorders early.

The study concluded that combination therapy with topical corticosteroids and hydroxychloroquine or finasteride is effective in treating Frontal fibrosing alopecia in Asians.

Ethnic Indian women with PCOS often have early symptoms, delayed diagnosis, and need better information and support for treatment and lifestyle management.

Early diagnosis and treatment of Kaposi varicelliform eruption are crucial to prevent severe complications.

Children and adults with Cushing's disease show different symptoms and males have more severe cases; surgery outcomes can be predicted by certain factors.

Androgenetic alopecia in teens is linked to obesity and other metabolic risks, needing early diagnosis and management.

Alopecia Areata has no cure, treatments are limited, and the condition often recurs, but new therapies like JAK inhibitors show promise.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

The document concludes that alopecia areata is an autoimmune disease without a definitive cure, but treatments like corticosteroids are commonly used.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

Some skin conditions may indicate metabolic syndrome, which could help with early detection and management of related health issues.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

A child with a rare vitamin D-resistant condition improved with treatment.

Trichotillomania in dementia may be better treated with dopamine blockers like quetiapine than with SSRIs.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Hyperthyroidism can hide signs of high androgen levels in females.

Most youth with gender dysphoria received hormones, had minor complications, and showed a decrease in suicide attempts after treatment.

RNA delivery is best for in-body use, while RNP delivery is good for outside-body use. Both methods are expected to greatly impact future treatments.

Certain skin symptoms can help detect and manage systemic lupus.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

No link found between new male baldness genes and female hair loss.

Some vaccines might rarely cause hair loss, more research is needed.

Effective hair loss treatment in women requires correct diagnosis and can include medications like minoxidil, antiandrogens, and treatments for underlying conditions like PCOS.

Six new hair loss factors in men not linked to female hair loss.

No link found between aromatase gene and female hair loss.