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The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Finasteride effectively treats mild to moderate hair loss in men aged 18-41, with some side effects.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Bicalutamide may help treat female pattern hair loss.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A child with a rare vitamin D-resistant condition improved with treatment.

Enhancers and super-enhancers are key in controlling specific gene activity and can play a role in cancer development.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

Narrowband UVB therapy significantly improved a child's rare skin condition.

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.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

CCT128930 is a promising new drug that effectively targets and inhibits a cancer-related protein, showing potential for cancer treatment.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.

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.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

More research is needed to understand how testosterone is maintained in adult males.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

Cri-du-chat syndrome can cause skin and oral lesions affecting nutrition and quality of life.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Certain vitamins in wrong amounts, alcohol abuse, metals, and other toxins can cause serious brain and nerve damage.

Female pattern hair loss is different from male pattern hair loss and has unclear genetic causes.

Hormone treatment for transsexual individuals is effective but carries risks like thromboembolic events and mood changes, with most side effects being minor and reversible.