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

Oxidative stress and immune dysfunction are linked to both Hashimoto's thyroiditis and polycystic ovary syndrome, with diet and specific treatments important for managing these conditions.

Ripretinib is effective and safe for treating advanced GIST in Chinese patients, particularly for non-gastric GISTs.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

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.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

Dutasteride, usually used for prostate issues and hair loss, could potentially treat Amyotrophic Lateral Sclerosis (ALS) due to its neuroprotective, antioxidant, and anti-inflammatory properties, but more testing is needed.

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

Understanding how acne develops in different diseases could lead to new treatments.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

Eating less can improve stem cell function and increase lifespan.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

The meeting highlighted major advances in skin research, including new findings on skin microbes, genetic links to skin diseases, and improved treatments for various conditions.

VEGF helps squamous cell carcinoma grow in ways beyond just blood vessel formation.

A girl with a rare skin condition improved after one month of treatment with acitretin.

Haircuts and medical growth factors do not cause cancer.

Malignant melanoma is the deadliest skin cancer, while BCC is the most common but rarely spreads, and SCC is more aggressive than BCC.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

Disrupting natural body clocks increases the risk of developing type 2 diabetes.

Minoxidil improved hair growth in a child with a rare genetic disorder.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

The enzyme Rand protease works well for leather dehairing and its stability is important, with Leu75 playing a key role.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.