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Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

The model and estimator can predict drug exposure in kidney transplant patients well.

Botox increased hair count in men with baldness and might work by improving scalp blood flow.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

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.

Products should be called 'sperm-safe' only after thorough, well-designed tests.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Hydrogels combined with extracellular vesicles and 3D bioprinting improve wound healing.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Custom-designed implants effectively repaired skull damage in most soldiers injured in combat.

The new FDA labeling rules provide more detailed drug safety information for pregnant and breastfeeding women, but more data is needed on the risks of many dermatologic drugs.

Operative hysteroscopy is still the main treatment for Asherman syndrome, but more research is needed on post-surgery methods.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Sostdc1 controls the size and number of hair and mammary gland structures.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The document concludes that Functional Hypothalamic Amenorrhea should be carefully diagnosed and managed to prevent health complications, using lifestyle changes and specific medications.

Early treatment of acne is crucial to prevent scarring and psychological effects.

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.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

PRP therapy helps heal pediatric surgical wounds faster and with fewer scars but needs more research for safety and cost.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Regenerative cellular therapies show promise for treating non-scarring hair loss but need more research.

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