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Amenorrhea, or the absence of periods, should be evaluated by age 15 or within five years of early breast development, and is most commonly caused by conditions like polycystic ovary syndrome and hypothalamic amenorrhea.

Selective breeding caused the unique curly hair in Mangalitza pigs.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

The document concludes that early diagnosis and treatment are crucial for managing rare hair loss disorders and that more research is needed to improve treatment strategies.

Contact immunotherapy might help treat various skin conditions, but more research is needed to confirm its safety and effectiveness.

Gene mutations can cause problems in male genital development.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Dlx3 is essential for hair growth and regeneration.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

The 2023 guideline for PCOS suggests using updated diagnostic criteria, assessing related health risks, and recommends lifestyle changes and specific treatments for symptoms and fertility issues.

The 2023 guideline advises a detailed approach for PCOS, focusing on early detection, lifestyle and medical treatments, and managing health risks.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Hair loss in men treated best with early medication or transplant, new treatments researched.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

EDA2R gene linked to hair loss.

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

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Non-coding RNAs play key roles in the hair growth cycle of Angora rabbits.

The conclusion is that exogen is a unique hair cycle phase and the new sampling method specifically targets this stage, which may help in future hair loss research.