Search

everythinglearnresearchcommunity

for

Search:↓

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Hypothyroidism may cause certain types of hair loss.

PCOS is a hormonal disorder causing symptoms like irregular periods and acne, and increases the risk of diabetes and heart disease.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

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

Understanding hair growth involves complex factors, and more research is needed to improve treatments for hair loss conditions.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

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

The conclusion is that formalizing how past decisions influence current health technology assessments could improve the credibility and defense of coverage decisions.

Different types of Armillaria fungus have a high genetic variety when partnering with Polyporus umbellatus mushrooms in China.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

The conclusion is that hair loss from CCCA may be genetic and not solely caused by hair grooming practices.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

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

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

Traditional knowledge of edible oil-producing plants in Sinja Valley is declining due to outmigration and sociocultural changes.

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

Many people in Majmaah city, Saudi Arabia, don't know much about vitamin D deficiency and don't practice good vitamin D habits, with few linking it to hair loss.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Chitosan nanoparticles are promising for sustained caffeine delivery through the skin.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

PCOS is a genetic disorder affecting women's reproductive health, with treatments focused on symptoms like insulin resistance and fertility.