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Aleglitazar and its major metabolite are safe enough to proceed to Phase 3 clinical trials.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Hormones control reproduction and are crucial for body balance.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

Babies were mostly born healthy from fathers who took finasteride, but some pregnancies ended early; more research is needed.

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

Early-onset baldness is linked to genetics, lifestyle, and can indicate higher risk for heart and metabolic diseases, and affects mental health.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

No single biomarker is reliable enough for diagnosing and assessing SLE.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Early skin biopsy helps diagnose and manage severe skin conditions in babies.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

High aldosterone and free testosterone levels link to female hair loss; testing aldosterone may predict hypertension risk.

Bicalutamide may help treat female pattern hair loss.

FGF13 gene changes cause excessive hair growth in a rare condition.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Eating a Mediterranean diet and taking certain supplements may improve symptoms of PCOS.

A gene mutation in Lama3 is linked to a common type of hair loss.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

Gastric bypass surgery improved a woman's hormonal disorder without the need for medication.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Understanding how androgens and their receptors work can lead to improved treatments for skin diseases.