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Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

A 44-year-old woman with Down's syndrome was diagnosed with both rheumatoid and gouty arthritis and treated with multiple medications.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

EDA2R gene linked to hair loss.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

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

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Mutations in the KRT85 gene cause hair and nail problems.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Six new hair loss factors in men not linked to female hair loss.

An 81-year-old man's white hair began to regain its original color while he was treated with lenalidomide, suggesting that graying hair might be reversible.

No link found between new male baldness genes and female hair loss.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Certain gene variations might be linked to severe acne in women but not in men.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

A new method can almost perfectly distinguish adenomyosis from similar conditions using blood tests.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.