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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.

Taking Propecia might lead to the development of 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.

Procyanidin B-2 is safe to use on skin as a hair growth product.

Interferons are effective for some skin conditions and cancers, but can have side effects and need more research for optimal use.

Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

New cancer treatments are less harmful to hair but can still cause hair loss, color, shape, and growth changes.

Most patients with Tuberous sclerosis had neurological or skin issues, and over half had psychiatric problems.

Yellow dots look different in various hair loss conditions and can help diagnose them.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

Different hair protein amounts change the strength of keratin/chitosan gels, useful for making predictable tissue engineering materials.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The research identified genes that explain why some sheep have curly wool and others have straight wool.

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

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

Stopping S100A3 activity slows down hair growth in mice.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

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

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.

Finasteride treats enlarged prostate and hair loss, but may cause side effects in some patients.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Androgen is important in controlling stem cell differentiation, reducing fat development, and increasing lean mass.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.