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Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Six genetic conditions are often linked to complete scalp hair loss in children.

The vitamin D receptor helps regulate skin and hair health independently of its usual vitamin D ligand.

Arteannuin might work against cancer and Alzheimer's by targeting neprilysin.

Early skin biopsy helps diagnose and manage severe skin conditions in babies.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

Different hair and scalp disorders cause hair loss or excess hair growth, with various treatments available depending on the specific condition.

Looking at skin can help find and treat serious diseases early.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.

A young man with an eating disorder had a life-threatening adrenal crisis due to an autoimmune condition, highlighting the need for better education on managing hormone treatments.

5α-reductase inhibitors and alpha-1 adrenergic antagonists together effectively treat benign prostatic hyperplasia, with long-term benefits.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Different types of hair loss in dogs and cats have various causes and treatments, with outcomes ranging from good to uncertain.

Alopecia in animals can be hereditary, congenital, or acquired, with treatments and outcomes varying widely.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

Eating the right nutrients can improve hair health, but taking extra supplements usually doesn't help unless you have a deficiency.

Gintonin-enriched fraction promotes hair growth and could be a potential alopecia treatment.

Autoimmune hepatitis in children often affects girls and can be treated successfully with medication.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

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