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Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Amenorrhea is relatively rare and initial testing should check FSH, TSH, and prolactin levels.

The three estrogen receptor genes are highly expressed in zebrafish neuromasts during development.

Fat tissue cells are a promising option for healing various diseases, but more research is needed to ensure they are safe and effective.

Women with PCOS often have skin problems like excessive hair, acne, hair loss, and dark patches, which can be treated with hormonal and non-hormonal therapies.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

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

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

Chronic Telogen Effluvium is a hair loss condition in middle-aged women that usually doesn't lead to complete baldness.

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

The document concludes that skin biopsies, genetic and environmental factors, and specific treatments are important in managing cutaneous lupus erythematosus.

Biotin treatment can significantly improve hair loss and motor functions in certain metabolic disorders.

Some women with common hair loss may develop permanent hair loss.

Dermatologists need to understand African American hair-care practices to better treat their hair and scalp disorders.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Minoxidil and finasteride treat hair loss; more research needed for other options.

Insulin resistance may contribute to various skin diseases and treating it could improve skin health and prevent more serious conditions.

Topical drugs and near-infrared light therapy show potential for treating alopecia.

Hair loss from Telogen Effluvium usually gets better within 6 months after addressing the cause.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

SAHA syndrome is a condition in women involving skin and hair issues, often related to hormonal imbalances, and is treated based on the underlying cause.

Vitamin D3 affects cell differentiation in specific skin areas.

PRP and HF-MSCs treatment improves hair growth, thickness, and density in androgenetic alopecia.

FFA's causes may include environmental triggers and genetic factors.

Nuclear hormone receptors play a significant role in skin wound healing and could lead to better treatment methods.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

Hormones and genetics affect hair growth and patterns, with some changes reversible and others not.

The document concludes that careful evaluation is key to diagnose and treat women with hair loss, with tests for thyroid, iron, and hormones as needed.