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Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

Finasteride may negatively affect male fertility.

Normal levels of DHT can reduce belly fat and increase muscle, but too much can lead to hair loss, prostate issues, and possibly heart disease.

Amenorrhea, or the absence of periods, should be evaluated by age 15 or within five years of early breast development, and is most commonly caused by conditions like polycystic ovary syndrome and hypothalamic amenorrhea.

In Japan, sex reassignment surgery for gender identity disorder faces challenges and needs better medical support and education.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

Scientists created keratinocyte cell lines from human hair that can differentiate similarly to normal skin cells, offering a new way to study skin biology and diseases.

Embryonic and adult stem cells are valuable for improving skin grafts and cell therapy.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Estrogen and prolactin may play bigger roles in female hair loss than previously thought.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

New treatments for prostate cancer and BPH show promise, including novel compounds that target hormone synthesis and response.

The critique suggests that Wilton's work unintentionally supports the very stereotypes it aims to question and calls for a broader, more inclusive approach to understanding gender.

Botulinum toxin A can help improve thin endometrium and embryo implantation.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

The document concludes that HAIR-AN syndrome should be considered when a patient shows severe hyperandrogenism and insulin resistance after excluding tumors.

miR-182 may help treat hallux valgus by targeting FGF9.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

Low doses of Asiasari radix extract boost stem cell growth without changing their shape.

Early treatment of acne is crucial to prevent scarring and psychological effects.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

CCL5 is important for the hair growth potential of human dermal papilla cells.

Most 46XX CAH patients have female identity, but a few identify as male and may need treatment and surgery.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Generalized glucocorticoid resistance causes hormone imbalances and varied symptoms due to gene mutations.

Umbilical cord and cord blood stem cells are promising for treating chronic diseases due to their versatility and ethical acceptability.

Azelaic acid helps with skin pigmentation issues, but its full effects are not completely understood.

PCOS is a complex condition that affects women's hormonal balance and metabolism, requiring lifestyle changes and medical management.