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Dentists should start preventive treatments early for children with Ichthyosis Vulgaris to avoid dental problems.

Skin problems are very common in people with end-stage kidney disease.

Lifestyle changes are the main treatment for PCOS, which is a complex condition requiring early management to reduce its health impacts.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Acne is a common skin condition that can be influenced by diet, lifestyle, and hormones, and requires a treatment approach that includes psychological considerations.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

Acne vulgaris is a common skin condition that can cause low self-esteem and depression, and early treatment is important to prevent scarring.

A new gene mutation causes insulin resistance in a girl and her mother.

The document is a detailed guide on skin conditions and treatments for dermatologists.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.

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.

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.

Researchers created a model to understand heart aging, highlighting the role of microRNAs and identifying key genes and pathways involved.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

The conclusion is that different blood diseases cause specific oral symptoms and require varied treatments to manage these symptoms and improve patient health.

Androgens and androgen receptors are important for metabolic health, affecting how the body uses glucose and fats through mitochondrial function.

A 21-year-old male has a benign skin condition called Becker's nevus, which he chose not to treat.

Ice-skating athletes often have skin problems due to cold, infections, and inflammation, needing careful treatment and prevention.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Eruptive vellus hair cysts are rare and often misdiagnosed, requiring biopsy for accurate diagnosis.

Hair graying may be caused by stem cell depletion from stress or melanocyte damage.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Minoxidil and Finasteride are effective for male baldness; more research is needed for hair aging treatments.

Hair loss in middle-aged women is often linked to insulin resistance and a family history of hair loss, particularly from their fathers.

Bioengineering can potentially treat hair loss by regenerating hair follicles and cloning hair, but the process is complex and needs more research.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.