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

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

Skin issues can indicate immune system problems.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Dihydrotestosterone makes arteries stiffer in female mice by reducing estrogen receptor expression.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

A 10-year-old boy with abnormal genital development had surgery and tests to find the cause and plan treatment.

Stem cell research and regenerative medicine have made significant advancements in treating various diseases and conditions.

Overexpressing Tβ4 in goats' hair follicles increases cashmere production and hair follicle growth.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

Adipose-derived stem cells show potential for skin rejuvenation and wound healing but require more research to overcome challenges and ensure safety.

Regenerative cellular therapies show promise for treating non-scarring hair loss but need more research.

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

Women with early-onset baldness should be checked for early bone loss, but bone density doesn't change with baldness severity.

Hair loss in women may have causes other than hormones.

The conclusion is that lifestyle changes and weight loss are first-line treatments for infertility due to anovulation, with various medications and assisted reproductive technologies as additional options.

5α-reductase inhibitors and alpha-1 adrenergic antagonists together effectively treat benign prostatic hyperplasia, with long-term benefits.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

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

Hair loss in women may have multiple causes, and eyebrow regrowth possible with specific injections.

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

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

Human hair follicle cells can be successfully transformed into different types of cells, but not more efficiently than other adult cells.

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

The document tests knowledge and decision-making in hematology through multiple-choice questions.

The document provides 70 multiple choice questions to improve haematology skills.

The first pediatric case of naevus trichilemmocysticus was documented.