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The 2003 consensus updated PCOS diagnosis criteria and highlighted increased risks of diabetes and heart disease for those affected.

The 2003 consensus updated PCOS diagnosis criteria and linked PCOS to higher risks of diabetes and heart problems, recommending lifestyle changes to lower these risks.

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

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Hormone imbalances can cause specific skin changes, which may help in early detection of endocrine disorders.

Some skin diseases and their treatments can negatively affect male fertility.

Hirsutism is too much hair growth in women like the pattern in men, often caused by high male hormones, and can be treated with hormone control and hair removal methods.

Testosterone is crucial for development, growth, and various body functions in mammals.

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

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

A young girl had a rare neck cyst removed and needs careful monitoring for related health issues.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

Polycystic ovary syndrome and iron overload share similar symptoms and can be potentially treated with blood removal, diet changes, and probiotics.

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.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Doctors should diagnose hair loss by examining the patient and possibly doing tests, and then treat it based on the type, which may prevent permanent hair loss.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

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

Androgens contribute to common male hair loss; more research needed for hair growth medication.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.