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Transdermal testosterone can improve sexual desire in postmenopausal women but lacks long-term safety data and is not FDA-approved for this use.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

CXCL12 protein slows down hair growth through its receptor CXCR4. Blocking this can potentially increase hair growth.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

The removed ovarian tumor was a rare type of blood vessel tumor that improved the patient's symptoms and hormone levels after surgery.

Transplanting one's own hair follicle cells can improve hair loss in men and women, and is particularly effective in women.

The woman's skin condition improved with specific oral and topical treatments.

Ch55 may help reduce skin scarring and fibrosis.

The patient's hair has unique structural differences with alternating bright and dark bands.

The infant was diagnosed with Rothmund-Thomson syndrome, a rare genetic disorder causing various physical and developmental issues.

A rare hair follicle disorder can cause itchy, bluish-black bumps on the body.

Eyelashes are important for looks and eye protection, and more people are treating sparse eyelashes; more research is needed to understand eyelash biology and improve treatments.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Human growth factor 20 can boost mouse whisker growth.

Krox20 overexpression in fibroblasts may play a role in abnormal scar formation and could be a target for new treatments.

Early treatment of hair-pulling disorder is crucial to prevent permanent hair loss and scarring.

Patients with PCOS rate their hirsutism higher than clinicians, and these self-ratings are more closely related to their quality of life and risk of depression.

A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

A woman's ovarian tumor causing high testosterone was successfully removed, and her symptoms improved.

A young girl had a rare neck cyst removed and needs careful monitoring for related health issues.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

A 5-year-old girl with a rare skin disorder was effectively treated with skin creams instead of oral medication.

Hormones and metabolism play a complex role in prostate enlargement, and more research is needed to improve diagnosis and treatment.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

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

Accurate diagnosis of NLS with dilated hair follicles is crucial to distinguish it from other conditions.