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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.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

A specific immune response helps control mite populations on the skin, maintaining healthy hair follicles.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Activating β-catenin increases melanocytes and decreases Schwann cells.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Skin healing from blisters can delay hair growth as stem cells focus on repairing skin over developing hair.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

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

The document is a detailed medical reference on skin and genetic disorders.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

The document explains various skin conditions and their treatments.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Eyelashes are important for looks and eye protection, and more people are treating sparse eyelashes; more research is needed to understand eyelash biology and improve treatments.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

Gene mutations can cause problems in male genital development.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Terbinafine is more effective than itraconazole for toenail fungus, especially in older patients, and debridement improves its effectiveness.