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Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Simvastatin may help manage symptoms in women with non-classic congenital adrenal hyperplasia by lowering cholesterol and certain hormone levels.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

The most common causes of hair loss in Jordanian children are fungal infections, autoimmune hair loss, and hair shedding after fever, with zinc deficiency also being a notable cause.

A rare gene variant causes hair and nail issues in a family.

The four main causes of hair loss in children are fungal infections, pulling out hair, autoimmune hair loss, and stress-related hair shedding.

Two babies needed surgery to remove hair tightly wrapped around their toes to prevent serious injury.

A woman with a rare adrenal tumor and hormonal disorder had improved testosterone levels after surgery, but her menstrual irregularities continued.

Lack of cystatin M/E causes thin hair and dry skin.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Antigens from skin cells may cause hair loss in perinevoid alopecia.

Alopecia in dogs is often caused by mange, flea and tick infestations, and nutritional deficiencies, especially in males and young dogs.

A new gene variant causes glucocorticoid resistance in a mother and son.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

Finasteride improves hair loss in women with hyperandrogenism.

Loss of keratin K2 causes skin problems and inflammation.

Certain genetic variants in keratins increase the risk of tooth decay.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

A new system helps better diagnose and treat female androgenization conditions like PCOS.

HDPCM treatment healed a baby's congenital skin defect caused by varicella infection.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Excessive blow-drying can cause "bubble hair," leading to hair loss and fragility, but improves when heat use is reduced.

N-WASP is essential for healthy skin and preventing inflammation.

A rare scalp condition mainly in older women can be treated with various alternatives to steroids, which may have fewer side effects.

Decreased IGF-1R expression may contribute to sacrococcygeal pilonidal sinus development.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Women with only irregular periods or excess hair have a better hormone profile than those with full PCOS, but both groups are similar, indicating a need for better PCOS diagnosis methods.

Some COVID-19 patients have different skin problems, which might be the only sign of the virus or related to other health issues.