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A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

The study identified key genes that regulate the growth cycle of cashmere in goats, which could help improve breeding strategies.

The document concludes that changes in eyelashes and eyelid skin can indicate various local and systemic diseases.

These methods help understand DNA changes in mouse skin.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Pregnancy can cause skin changes and affect existing skin conditions, with limited treatment options due to the need for fetal safety.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

The conclusion is that lifestyle changes and weight loss are first-line treatments for infertility due to anovulation, with various medications and assisted reproductive technologies as additional options.

Hair loss in balding individuals is linked to changes in specific hair growth-related genes.

Men with hair loss have more DNA changes in back-of-head hair follicles, possibly protecting them from thinning.

Alopecia areata involves immune response and gene changes affecting hair loss.

Some drugs can cause skin and hair color changes, often reversible when the drug is stopped.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Doxazosin mesylate and saw palmetto cause genetic changes in fruit flies.

The document concludes that skin and nail changes can indicate various underlying health conditions.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

The conclusion is that androgenetic alopecia and senescent alopecia have unique gene changes, suggesting different causes and potential treatments for these hair loss types.

The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

Animals that change color with the seasons mainly do so in response to daylight changes, but climate change is causing camouflage problems that may require evolutionary changes.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

Childhood obesity is rising globally due to various factors, and early prevention and healthy lifestyle changes are crucial.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

The document concludes that managing female hyperandrogenism requires a combination of identifying the cause, lifestyle changes, medication, and cosmetic treatments.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Polycystic Ovary Syndrome (PCOS) is a common condition in women that can cause metabolic, reproductive, and psychological issues, and requires lifestyle changes and medication for management.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

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.