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The Consciousness Energy Healing Treatment significantly increased human dermal papilla cell growth, suggesting it may help with hair growth and skin disorders.

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

Hormone therapy is essential for transgender individuals but requires careful management due to possible metabolic effects.

New genes and pathways are important for testosterone production and male sexual development.

The book is recommended for its new scientific information and balanced treatment options for hair loss in domestic animals.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

The French Endocrine Society suggests diagnosing PCOS with two of three signs, recommends lifestyle changes and clomiphene for treatment, and calls for more research on certain treatments and tests.

A woman with breast cancer developed a rare condition causing excessive fine hair growth on her face and body.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

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

SCF and ET-1 together significantly increase skin pigmentation and melanin production.

Sex hormones affect hair and feather growth and may help manage alopecia and hormone-dependent cancers.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Acne lesions start with changes in hair follicles and increase in inflammation, suggesting a cycle that could affect treatment strategies.

Metabolic syndrome in kids and teens is linked to obesity and increases diabetes and heart disease risk; early lifestyle changes are crucial for management.

The superficial temporal artery flap is a reliable method for reconstructing complex facial defects with minimal complications.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

CBG may help with various medical conditions but needs more human research to confirm safety and effectiveness.

New treatments for hair loss show promise, but more development is needed, especially for tough cases.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

Post-finasteride syndrome causes sexual, physical, and psychological symptoms, but more research is needed to understand its causes and connection to finasteride.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

Pili anulati may cause hair loss, proper diagnosis and treatment needed.

Vismodegib is effective for basal cell carcinoma but has severe side effects.

Men with early balding may have hormonal imbalances similar to women with PCOS and could benefit from similar treatments.