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A woman's rare benign tumor that released both cortisol and testosterone was successfully removed, improving her health.

Melanocytes are important for normal body functions and have potential uses in regenerative medicine and disease treatment.

Pregnant women with PCOS have higher levels of Neurokinin B in the placenta, especially with female babies.

A pineal tumor caused a boy's early puberty, which changed from peripheral to central after treatment.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Hyperandrogenism is a common hormonal disorder in women, often linked to PCOS.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

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

The document encourages attending the 2023 Dermatology Nurses' Association Convention.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

A woman's new seizures were caused by a brain tumor likely linked to her past cancer treatment, and choosing safe seizure medications is important for women who can have children.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Protein profiling of forehead skin can help distinguish between frontal fibrosing alopecia and androgenetic alopecia.

Retinoids are important for treating skin conditions but should be used with caution due to serious side effects and risks during pregnancy.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

A newborn with congenital syphilis had unusual hair loss possibly caused by the infection.

The top research priorities for congenital ichthyosis include long-term side effects of oral retinoids, best topical treatments, and treatments for itch and hair loss.

Woolly hair is a rare genetic condition with no effective treatments.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

The book is a valuable reference on androgenic disorders for professionals but not suitable for laypeople or medical students.

Skin symptoms are important for diagnosing infections in children.

The document concludes that non-scarring alopecias can be reversed, but scarring alopecias cause permanent hair loss.

Treat pediatric skin issues with accurate diagnosis, multidisciplinary team, and various treatment options.

Different hair care practices and conditions affect African American hair and scalp health, requiring specialized knowledge for treatment.