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Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Fat tissue stem cells may help increase hair growth.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

DHT, a testosterone byproduct, causes male pattern baldness.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Premature balding in some men may be linked to altered hormones, but it's not the male equivalent to polycystic ovary syndrome or metabolic syndrome.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Researchers found a gene mutation responsible for a rare hair loss condition.

A new mutation in the HR gene causes hair loss in a specific family.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

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.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

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.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Hair follicle development is controlled by interactions between skin tissues and specific molecular signals.

The guidelines suggest lifestyle changes, diet adjustments, and personalized medication to manage dyslipidemia and reduce heart disease risk.

Half of people with Alopecia Areata may see hair regrowth within a year without treatment, but recovery is unpredictable.

Human skin makes sexual hormones that affect hair growth, skin health, and healing; too much can cause acne and hair loss, while treatments can manage these conditions.