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High-resolution MRI can distinguish between tertiary androgenetic alopecia and severe alopecia areata by measuring scalp and tissue thickness and hair follicle depth.

Preventing cancer involves lifestyle changes, vaccinations, early screening, and understanding cancer's molecular basis.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Selective breeding caused the unique curly hair in Mangalitza pigs.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Blocking interferon-gamma might help treat various autoimmune diseases.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Reduced androgens linked to kinky hair disorder and hair loss; 5a-reductase inhibitors may help.

Paternal drug exposure can harm fertility, pregnancy outcomes, and offspring health, with specific drugs linked to various reproductive issues.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Forensic DNA phenotyping can help generate new leads in cold cases but faces accuracy, legal, and acceptance challenges.

Long non-coding RNAs help regulate wool fineness in Gansu alpine fine-wool sheep.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Combining fractional CO2 laser with topical dutasteride is more effective for treating male hair loss than using the laser alone.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

A pregnant woman with Werner's syndrome died during childbirth, but her baby survived and did not have the syndrome.

Any medication can cause skin reactions, some due to allergies and others due to dosage or genetic factors.

Hair relaxers are linked to reduced cystine levels and potential hair damage.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

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

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.