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A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Mutation in hairless gene may increase hair loss risk.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

t-Flavanone helps improve male pattern hair loss by making hair roots stronger.

Finasteride, often used for hair loss, can potentially cause cataracts.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

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

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Early diagnosis and aggressive treatment are crucial for Cicatricial Alopecia, and treatment effectiveness varies among patients.

The chapter explains the causes of excessive hair growth and masculinization in women and how to measure hormone levels related to these conditions.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Mutation in hairless gene may increase hair loss risk.

FLCN helps control iron levels in cells.

Some skin tumors from hair follicles and glands can be linked to genetic syndromes and may be benign or malignant.

Nutrease powder, a high-protein, low-carb supplement, can help manage Polycystic Ovary Syndrome symptoms, regulate periods, improve ovulation, and restore fertility.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Proper care and diet are crucial to prevent health issues in gerbils.

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

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

The conclusion is that using drugs to block the TOR pathway might slow aging and prevent age-related diseases.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Vitamin D and its receptor regulate skin functions like cell growth, immunity, hair cycle, and tumor prevention.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

Targeting androgen receptors could be a promising way to treat skin disorders with fewer side effects.

South Asian women with PCOS are more likely to have metabolic issues and central obesity, and simple measures like waist size and blood pressure can help identify these risks early.