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The conclusion is that modifying scalp lifting surgery by cutting one occipital artery and making other changes reduces complications and improves outcomes for patients with severe hair loss.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

The conclusion is that FFA and LPP have similar scalp biopsy features, making them hard to distinguish histologically, and FFA may be a specific kind of scarring hair loss.

The conclusion is that understanding how feathers and hairs pattern can help in developing hair regeneration treatments.

Women's ovarian hormones and adrenal androgens change throughout life, affecting hair loss and health.

A woman developed male traits from accidental contact with her husband's testosterone gel.

Finasteride helps protect brain in old male rats.

Different areas of the scalp have varying hair thickness, useful for different types of hair transplant needs.

Frontal Fibrosing Alopecia might be an autoimmune disease.

A U.S. Naval fighter pilot suffered permanent vision loss in one eye due to recurrent central serous retinopathy.

Hair loss can be an early sign of HIV infection.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

A woman's diabetes improved after removing ovarian tumors that caused high testosterone levels.

Early diagnosis and combination therapy, especially with finasteride and dutasteride, are key to managing Frontal Fibrosing Alopecia effectively.

Taiwan reported its first case of a rare scalp condition with no clear cause or treatment.

Finasteride use may cause sexual dysfunction; more research needed.

Wearing a wig caused a woman's skin condition to worsen due to pressure from the wig's fasteners.

Isoniazid can rarely cause hair loss, which is reversible after stopping the drug.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

MRI helps distinguish between pituitary adenomas and craniopharyngiomas, guides treatment for pediatric CNS tumors, and assesses rhinocerebral mucormycosis with a high mortality rate in transplanted patients.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Gene therapy with the Math1 gene helped regenerate balance-related cells and improve balance in mice.

Alopecia is a key indicator of thallium poisoning.

Choosing the right model order in brain connectivity analysis can affect the detection of differences between healthy individuals and those with seasonal affective disorder.

Voriconazole can cause serious side effects, especially in long-term use.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Excessive hair growth can be assessed by history, exam, and blood tests, and treated with medication like dexamethasone, birth control pills, and spironolactone.

Finasteride may help reduce symptoms in male Tourette syndrome patients.