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UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

More melanoblasts in hair follicles mean better survival and proper hair pigmentation.

Different types of PCOS need specific diagnosis methods and treatments.

Increased FGFR2b signaling, influenced by androgens, plays a role in causing acne.

The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

CBD may improve skin and hair health, but its effective use and safety need more research.

Adult acne is often related to hormonal disorders, especially in women, and may need long-term treatment involving specialists.

Down Syndrome patients with Alopecia Areata often have hypothyroidism and specific immune abnormalities.

Human beard hair medulla contains a unique and complex mix of keratins not found in other human tissues.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

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

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

Humans lost body hair relatively recently in evolution.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

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

Genetic differences may affect COVID-19 deaths; anti-androgens could be potential treatment.

Msx2 and Foxn1 are both crucial for hair growth and health.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.