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Severe insulin resistance can be managed with medication, lifestyle changes, and treatment for related conditions.

Peginterferon alfa-2b and ribavirin therapy for hepatitis C can cause serious side effects, some different from those reported in clinical trials.

Mice without collagen VI have slower hair growth normally but faster regrowth after injury.

Mice without certain skin proteins had abnormal skin and hair development.

Early onset hair loss linked to genetics and androgen levels.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Psychotropic medications can cause skin reactions, including severe conditions like SJS and TEN, and it's important for psychiatrists to recognize and manage these side effects.

Smad1 and Smad5 are essential for hair follicle development and stem cell sleepiness.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

New treatments for PCOS focus on insulin resistance and reducing testosterone levels, along with traditional hormone therapies.

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.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

Steroidogenic isoenzymes may help improve treatments for common hair loss.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Thai people's hair density decreases with age and varies by scalp area, but hair thickness stays the same regardless of age or scalp area.

Skin problems can be linked to sexual abuse, requiring careful medical and psychological evaluation.

Hedychium spicatum has medicinal properties but needs more research for scientific validation and use.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

BAF200 is essential for proper heart and coronary artery formation.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Oral zinc sulphate reduces dark hair color in mice.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

The Ovol2-Zeb1 circuit is crucial for skin healing and hair growth by guiding cell movement and growth.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Gata6 is important for protecting hair growth cells from DNA damage and keeping normal hair growth.

Understanding and tracking our body's natural daily rhythms could help improve heart health.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.