Search

everythinglearnresearchcommunity

for

Search:↓

Female pattern baldness may indicate a higher risk of coronary artery disease.

AGA is a genetic, hormonal hair loss treated with finasteride, minoxidil, and supplements, but new compounds are being developed.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

The document explains the genetic causes and characteristics of inherited hair disorders.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Polycystic ovarian shape is a genetic sign of PCOS and its hormonal and metabolic features can be inherited.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Male pattern baldness is often genetic and linked to a hormone, with treatments like finasteride and minoxidil being effective for some men.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

Collagen makes skin stiff, and preservation methods greatly increase tissue stiffness.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

A mother's diet at conception can cause lasting genetic changes in her child.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Oral sturgeon oil promotes hair growth and improves gut health.

Seborrheic alopecia in young people is linked to fungal infections, especially Malassezia.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

The document is a detailed medical reference on skin and genetic disorders.

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.