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Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

About 2.2% of women with symptoms of high male hormones have a mild form of congenital adrenal hyperplasia, and measuring a specific hormone level can accurately diagnose it.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

The definition of Polycystic Ovary Syndrome may change with new research, and careful screening is key for managing the condition.

Correcting nutrient deficiencies may help with hair loss, but the benefits of supplements without a deficiency are uncertain and could be harmful.

Premature graying of hair may suggest health issues and currently lacks effective treatments.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Women with congenital adrenal hyperplasia have lower fertility, but with proper treatment, they can conceive successfully.

A new mutation in the HR gene causes hair loss in a specific family.

Lack of cystatin M/E causes thin hair and dry skin.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

ESR2 gene linked to female-pattern hair loss.

Women with non-classic congenital adrenal hyperplasia have higher risk for heart and metabolic problems.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

Patients often experience long-lasting changes to their hair after stem cell transplants.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Hormones, especially testosterone and DHT, are key for penis development and function, and testosterone therapy may help with erectile dysfunction in those with low levels.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Finasteride significantly increases scalp hair and prevents hair loss in young and middle-aged men.

Biotin supplements may improve hair and nail growth in people with certain deficiencies or conditions, but there's not enough evidence to recommend it for healthy individuals.

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

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