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Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

Diffuse alopecia in women may be related to androgens and iron deficiency, and basic hormone and nutrient screening is useful.

PCOS is a common condition in women that can lead to infertility and other health issues, and it's diagnosed by specific criteria with various treatment options available.

The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.

Epigenetic changes control how adult stem cells work and can lead to diseases like cancer if they go wrong.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Changes in skin microbes play a role in some skin diseases and could lead to new treatments.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

FPHL is a common, age-related, genetic hair loss with unclear causes and limited treatment options.

Lifestyle changes are the main treatment for PCOS, which is a complex condition requiring early management to reduce its health impacts.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Despite progress, better treatments and understanding are needed for the high rates of long-term issues and deaths linked to eating disorders.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

Different genes cause Female Pattern Hair Loss compared to male hair loss, and treatments vary, but more research is needed to understand it fully.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

The complement system might be involved in the development of alopecia areata and could lead to new treatments.

Genes controlling hair growth and immune response are disrupted in male pattern baldness.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Understanding where cancer cells come from helps create better prevention and treatment methods.

Mutation in hairless gene may increase hair loss risk.

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.

The conclusion is that a systematic approach is key for treating symmetrical alopecia in dogs, but treatment may not always be necessary.

Mutation in hairless gene may increase hair loss risk.

AGA more common in men, Koreans have lower rates and unique patterns.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

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

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.