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New treatments for male hypogonadism are effective and should be personalized.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

Fetal cells could improve skin repair with minimal scarring and are a potential ready-to-use solution for tissue engineering.

Low serum complement levels in SLE patients don't always match with disease flares; monitoring C3 and C4 is useful, but cell-bound complement products might better indicate disease activity.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.

Testosterone therapy seems safe and effective for transgender men with proper care, but more long-term research is needed.

ISCK03 stops melanin production in human melanoma cells and lightens skin color in mice and guinea pigs.

Larger ovarian size is linked to higher insulin resistance in women with PCOS.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Rat dermal papilla cells have unique genes crucial for hair growth.

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.

Carvone helps treat skin issues by reducing melanin and stopping harmful cell growth.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

Dermoscopy is useful for many health professionals, not just dermatologists, in improving skin condition diagnoses and reducing unnecessary biopsies.

Lifestyle changes and clomiphene are first-line treatments for infertility in women with PCOS, with other options available if these fail.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Biologics for severe asthma have known side effects, but some new risks need more study.

The symptoms described align more with Haberland syndrome, not Delleman-Oorthuys syndrome.

The document concludes that careful history and physical exams are crucial for accurately diagnosing polycystic ovary syndrome and distinguishing it from other similar conditions.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Shorter PSADT after prostate surgery is linked to higher risk of death.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

While PCOS might increase the risk of heart disease, there's not strong evidence to prove it causes earlier heart problems.

Childhood obesity is rising globally due to various factors, and early prevention and healthy lifestyle changes are crucial.

Telocytes might help with skin repair and regeneration.

Postpartum depression is linked to changes in brain chemicals, inflammation, stress, and certain genes, and can potentially be identified by markers like specific steroids, serotonin levels, and vitamin D levels.

People with PCOS, especially if obese, often have NAFLD, linked to obesity, insulin resistance, and high androgen levels.

The document concludes that understanding the sebaceous gland's development and function is key to addressing related skin diseases and aging effects.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.