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A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Mutations in the AR gene cause hair thinning and loss.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

HOXC13 is essential for hair and nail development by regulating Foxn1.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Camellia japonica extract may improve scalp health and promote hair growth.

Uterine leiomyomas don't significantly change gene expression in the scalp of people with Central Centrifugal Cicatricial Alopecia.

Researchers successfully grew horse skin cells that produce pigment from hair follicle samples.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

The symposium highlighted the importance of genetics in understanding and treating complex skin diseases.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Hair samples can be used to create stem cells easily and non-invasively.

The complement system might be involved in the development of alopecia areata and could lead to new treatments.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

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.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

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

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.

EDA2R gene linked to hair loss.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

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