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Iron deficiency might contribute to hair loss in women.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Doxazosin mesylate and saw palmetto cause genetic changes in fruit flies.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Specialized ribosomes affect aging in human skin cells.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Low-dose acitretin helps nail psoriasis, stem cells may treat scarring alopecia, Chinese men have lower baldness rates, lateral foldplasty is good for ingrown toenails, hair diameter helps diagnose female baldness, childhood trauma linked to alopecia areata, certain hair-weaving leads to scalp conditions in African American women, and new methods for hair research and understanding hair and sweat gland development were introduced.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

The Hairless gene is crucial for healthy skin and hair growth.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Chromosomal changes, including those in the WRN gene and rDNA, may significantly contribute to aging.

A mouse gene mutation increases the risk of skin cancer.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Understanding hair follicle development can help treat hair loss, skin regeneration, and certain skin cancers.

Significant progress was made in understanding PXE, but effective treatments are still needed.

New hair growth corticosterone levels are higher in diabetic mice, indicating long-term stress.

Skin organoids from stem cells could better mimic real skin but face challenges.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Adult acne is often related to hormonal disorders, especially in women, and may need long-term treatment involving specialists.