Search

everythinglearnresearchcommunity

for

Search:↓

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Recognizing rare causes of MASLD is crucial for effective treatment and preventing complications.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Premature graying of hair is linked to vitamin D and B12 deficiencies, thyroid issues, iron imbalance, stress, and lifestyle habits, and affects quality of life.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Some skin diseases and their treatments can negatively affect male fertility.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

Skin problems in the elderly are unique and may indicate other diseases, involving changes in skin, hair, nails, and increased cancer risk.

A defective protein in progeria causes cell death and atherosclerosis, but a treatment targeting cell stress may reduce these effects.

Men's hair loss is caused by hormones and genes, and can be treated with medication and surgery, while graying is due to aging and has no prevention except dyeing.

Hair changes can indicate systemic diseases or medication effects.

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

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Premature graying and hair changes can be treated with certain peptides and possibly targeting the endocannabinoid system.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Some skin problems can be signs of diabetes or other metabolic diseases and recognizing them can help diagnose and treat these diseases early.

Hair color is influenced by genetics and can indicate certain health conditions.

Hair ages due to genetics and environmental factors, leading to graying and thinning, with treatments available for some conditions.

Hair loss has many causes and treatments, and losing some hair daily is normal; proper diagnosis is key, and minoxidil can help treat it.

Hair aging is caused by stress, hormones, inflammation, and DNA damage affecting hair growth and color.

Pediatricians should treat some hair loss types in children and refer others to a dermatologist.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Different connective tissue disorders have unique symptoms and treatments, with varying outcomes and often require ongoing care from a specialist.