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A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Testosterone is crucial for development, growth, and various body functions in mammals.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

Children's hair loss has many causes and requires careful diagnosis and personalized treatment, including emotional support.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Hormonal therapies are safe and effective for treating acne in female adolescents, with specific treatments for those with endocrine disorders.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Hirsutism, excessive hair growth in women, is often caused by PCOS and can be managed with medication and personalized treatment plans.

Healthcare providers should start with simple fertility tests and treatments before referring patients to specialists.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Telogen Effluvium is a hair loss condition where treatment involves identifying and managing its triggers.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Inducing ferroptosis in hepatic stellate cells is crucial for treating liver fibrosis.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

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

Some supplements may help with hair loss, but there's not enough strong evidence to recommend them without doctor advice.

Squarticles, tiny particles made from sebum-derived lipids, can effectively deliver minoxidil, a hair growth drug, directly to hair follicles and skin cells, with less skin penetration and more tolerability.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

New treatments for hair growth disorders are needed due to limited current options and complex hair follicle biology.

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

Severe acne in a young girl may indicate underlying hormonal issues.

Minoxidil was more effective than laser therapy for hair loss, and the report also highlighted the need for more research on PRP for a different hair loss condition, the impact of social media on alopecia views, and a warning on turmeric causing nail discoloration.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.