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The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Low and ultralow doses of flutamide can cause liver damage in young women with high androgen levels, regardless of dose or birth control use, with higher risk for those with higher BMI and liver enzyme levels before treatment.

The guideline recommends mental health involvement in diagnosing gender identity disorder and outlines hormone and surgical treatment protocols, emphasizing safety, informed consent, and long-term monitoring.

Lichen Planopilaris and Frontal Fibrosing Alopecia may help us understand hair follicle stem cell disorders and suggest new treatments.

Testosterone therapy and surgeries like mastectomy improve transgender men's lives and mental health with low risks and high satisfaction.

NGAL may help maintain skin balance and is linked to skin disorders and cancers.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

A woman with lupus experienced skin death due to a blood clotting disorder after stopping a blood thinner, which healed with treatment.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

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

Androgens play a key role in hair growth and disorders like baldness and excessive hairiness.

Societal pressure for the perfect body leads to health risks and disorders.

Hair follicle stem cells have significant potential for treating various disorders.

Hair follicle organoids can help study hair biology and disorders but need improvements for wider use.

Higher basal metabolic rate increases the risk of non-alcoholic fatty liver disease, especially in Chinese people, and may require tailored management.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Isotretinoin affects trace element levels and requires monitoring of liver and kidney functions.

Woodhouse-Sakati Syndrome can include unique symptoms like liver issues and low growth hormone.

Patients with RASopathies have a higher risk of autoimmune disorders and should be routinely screened.

The document is a detailed medical reference on skin and genetic disorders.

Patients with one autoimmune disease should be checked for other autoimmune disorders.

Androgen lowering medications don't significantly change HCV-related liver cancer risk in men.

Hair follicle biology advancements may lead to better hair growth disorder treatments.

Neuroactive steroids show promise for treating mental and neurological disorders by targeting GABA_A receptors.

The document suggests that clinical trials for PCOS should focus on meaningful primary outcomes like live birth rates, rather than less reliable surrogate markers.

New method uses hair follicle cells to estimate human body clock phase, potentially improving sleep disorder diagnosis.

Stopping minoxidil and draining fluid around the heart can save lives in rare cases.

Trilostane effectively improved symptoms in dogs with a certain adrenal gland disorder.