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A new gene variant in the DSP gene is linked to a unique type of hair loss.

The document explains the genetic causes and characteristics of inherited hair disorders.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

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

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Pica disorder in central Iraq is mainly found in females and is linked to low iron levels; treatment with iron improves most patients.

A young Saudi girl with uncontrolled type 1 diabetes and hypothyroidism had two rare conditions, Mauriac syndrome and Van Wyk–Grumbach syndrome.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Good nutrition is crucial for health and preventing disease, and supplements can help prevent nutrient deficiencies.

Early NAS level changes affect alcohol consumption vulnerability.

A woman experienced excessive hair growth after using a hair loss treatment with minoxidil.

The document concludes that transsexual individuals often experience improved quality of life after transitioning, despite higher risks of psychiatric issues and mortality.

The document concludes that low-dose acne treatment is most suitable for moderate acne, with high patient satisfaction and low relapse rates.

Primary care is key in managing PCOS, focusing on lifestyle changes and medications like birth control and metformin.

The meeting covered new findings in children's skin conditions and treatments, including the benefits of super absorbent polymer diapers.

Follistatin and LIN28B together improve the ability of inner ear cells in mice to regenerate into hearing cells.

JAK inhibitors are more effective and safer for treating alopecia areata than dupilumab and apremilast.

Oxytocin receptors are found in skin cells near touch and pain neurons.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

Vitamin B6 helps increase hair growth and density in rabbits by affecting certain cell signaling pathways.

Low selenium intake may delay puberty in boys but not in girls.

Sex and sex hormones can affect brain inflammation in Parkinson's disease, with male mice being more affected and female mice showing a protective effect.

Baricitinib improved platelet counts and alopecia in a 16-year-old with chronic immune thrombocytopenia.

A pineal tumor caused a boy's early puberty, which changed from peripheral to central after treatment.

TGF-β2 helps activate hair follicle stem cells by counteracting BMP signals.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

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

Biotin deficiency in patients on total parenteral nutrition can cause serious symptoms but can be treated with biotin supplements.