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The BASP classification is effective for diagnosing pattern hair loss in Indian men and women.

Early onset hair loss in young men is common and linked to family history and alcohol use.

AGA increased yearly, type I most common, and family history and seborrheic dermatitis often linked.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Plant-based remedies may treat hair loss by reducing inflammation and improving insulin resistance.

Hair loss in women can be slowed with treatment, but more research needed for better solutions.

The paper suggests that hair loss might be caused by skull growth, not just DHT's effect on hair follicles, and calls for more research.

At least 87% of Indian men experience hair loss, with type II being most common and severity increasing with age.

Early hair loss common in Chinese males, linked to family history and smoking; early treatment advised.

Most types of hair loss can regrow naturally, but there are no effective cures for male pattern or age-related hair loss, and only limited options for females.

Early-onset AGA shows different hair and metabolic characteristics compared to normal-onset AGA.

Future treatments for androgenic alopecia may focus on reactivating hair follicle stem cells and improving drug delivery.

Androgenetic alopecia is common in South-West Nigeria, affecting more men than women, with stress worsening the condition.

Different types of female pattern hair loss have unique characteristics and are associated with various health conditions.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

PCOS and related metabolic issues often run in families.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Ayurveda's descriptions of genetic disorders align with modern genetic understanding.

Genes and hormones cause hair loss, with four genes contributing equally.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Cantú syndrome may be linked to pituitary adenomas.

Eating vegetarian, having allergies, and family history might be linked to getting gray hair early.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Male pattern hair loss is diagnosed and treated earlier and is milder, possibly due to early puberty.

Smoking linked to hair loss in Asian men.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.