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Early diagnosis and treatment of PCOS can prevent complications and improve symptoms.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Lichen planopilaris is a chronic, scarring hair loss condition with no definitive cure, requiring accurate diagnosis and treatment to manage symptoms.

Hormones, especially androgens, play a key role in acne, which can be a symptom of systemic diseases like PCOS and may require targeted treatment.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Long-term minoxidil use can cause pseudoacromegaly, but stopping it improves symptoms.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Permanent hair loss from cicatricial alopecia is treated by reducing inflammation and managing symptoms, but regrowth in scarred areas is unlikely.

The document concludes that careful evaluation is needed to diagnose PCOS correctly due to similar symptoms in other conditions, and accurate testosterone level measurement is crucial.

Seven patients were misdiagnosed with discoid lupus instead of lichen planopilaris due to similar symptoms, showing the need for careful diagnosis in scarring hair loss conditions.

Some women with Frontal Fibrosing Alopecia also have Lichen Planopilaris, which can lead to more symptoms and affect hair outside the scalp.

Some recovered COVID-19 patients experience skin, hair, and nail issues, suggesting they need follow-up care.

New signs like changes in blood markers, physical symptoms, and behavioral shifts may help detect hidden steroid use in athletes.

A woman's ovarian tumor causing high testosterone was successfully removed, and her symptoms improved.

Early treatment and weight management are important for teenagers with PCOS to reduce symptoms and long-term health risks.

Effective treatment significantly improves pododermatitis in dogs, reducing symptoms and extending remission.

Keloids significantly reduce quality of life, and treating symptoms should be prioritized.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

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

Platelet-rich Plasma Gel may help treat en coup de sabre scleroderma, improving symptoms and skin quality with minimal side effects.

PCOS is a genetic disorder affecting women's reproductive health, with treatments focused on symptoms like insulin resistance and fertility.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

The guideline suggests using specific criteria to diagnose PCOS, recommends various treatments for its symptoms, and advises screening for related health issues.

Experts recommend using evidence-based methods to diagnose and treat hirsutism, focusing on symptoms and underlying causes.

Kawasaki Disease is rare and often missed in adults, who show different symptoms than children, and may benefit from early treatment.

Excessive hair growth in women often has no known cause and is not linked to race or other hormonal symptoms.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

Finasteride effectively treats enlarged prostate and male baldness, improves symptoms of hirsutism in women, but doesn't work for acne, and may delay prostate cancer progression with few side effects.

Vitamin B12 deficiency can cause skin darkening and increased blood vessels, but treatment can improve symptoms.