Search

everythinglearnresearchcommunity

for

Search:↓

The review concludes that more research is needed to better improve the health outcomes for people with Polycystic Ovarian Syndrome.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Twins had rare skin cysts likely due to genetics.

Improving knowledge and practices in animal fibre production is crucial to meet market demands and potentially revive natural fibres.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

A man with testotoxicosis was fertile despite low FSH levels, suggesting high testosterone may allow sperm production without FSH.

Oxidative stress may contribute to hair loss in alopecia areata and antioxidants could potentially help as a treatment.

A 66-year-old woman's thick scalp and hair loss were confirmed as lipedematous alopecia, a rare condition possibly influenced by genetics, with no effective treatment known.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Mutation in hairless gene may increase hair loss risk.

Alopecia Areata is an autoimmune condition causing hair loss, influenced by genetics, environment, and possibly improved by anti-MIF therapy, with many patients experiencing regrowth within a year.

Understanding skin structure and development helps diagnose and treat skin disorders.

Any drug can cause skin reactions, but antibiotics, NSAIDs, and psychotropic drugs are more common, with some reactions being life-threatening.

Early treatment of PCOS in teens is crucial to prevent long-term health issues like diabetes and heart disease.

Alopecia areata is an autoimmune disease with genetic links, treatable with certain medications, and can affect mental health.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

Neuroactive steroids may affect the risk and treatment of alcohol use disorders.

Heredity and hormones cause common hair loss, and topical minoxidil is the first recommended treatment.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

Genetic factors could lead to personalized treatments for hair loss.

The Middle East and Africa need better data, treatment consensus, and support for Alopecia Areata.

Custom skincare can be made based on genes, fewer cats in Lublin have FeLV/FIV than national average, and studies also looked at small water bodies, river pollution, guppy growth, toxins in biochars, palm oil issues, and pumpkin seed oil for hair strength.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Hidradenitis Suppurativa is likely an autoinflammatory disease, and better understanding its causes could improve treatments.

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.

Alopecia areata in infants may be more common than previously thought.

Correct testosterone levels for age to treat prostate cancer, using low dose treatments as necessary.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.