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A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Hypothyroidism may cause certain types of hair loss.

Minoxidil and finasteride are effective for treating hair loss, with dutasteride showing potential but with side effects.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

KAP7.1 and KAP8.2 genes are crucial for cashmere quality in goats.

Ectodysplasin signaling is crucial for skin appendage development, requiring specific doses and durations.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Genetic factors and diet significantly increase the risk of male pattern baldness.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Dutasteride is more efficient than finasteride, but individual results vary.

Alopecia areata, a type of hair loss, may be passed through T cells and has genetic links, while treatments vary in effectiveness. Male pattern baldness can be treated with finasteride and is influenced by androgens in hair follicles.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

A new method helps detect androgen receptor movement in cells, aiding research on hair loss treatments.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Low-dose finasteride may cause fertility issues, but stopping it can improve sperm quality and lead to pregnancy.

Interferons are effective for some skin conditions and cancers, but can have side effects and need more research for optimal use.

People with Down's syndrome are more likely to have syringomas.

Epigenetic factors play a crucial role in skin health and disease.