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The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

Rare adrenal cancers that secrete androgens or estrogens have a poor prognosis and are treated primarily with surgery.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.

Women with PCOS and higher BMI, especially those with morbid obesity, are at greater risk for depression.

The document concludes that diagnosing and managing plaque psoriasis, particularly in sensitive areas, is challenging and requires careful differentiation from similar skin conditions.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

Minoxidil improved hair growth in a child with a rare genetic disorder.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

The document concludes that various skin conditions have specific characteristics and treatments, and highlights the importance of vitamin D in managing these dermatological issues.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

Testosterone therapy helps boys with hormone deficiencies develop normal male characteristics and grow properly.

Hair aging and loss are caused by genetics, hormones, environment, and grooming, with treatments like minoxidil effective for certain types of hair loss.

Hair loss is caused by genetics and hormones, diagnosed through examination and biopsy, and treated with medications or surgery.

Hormone therapy may increase migraines in transgender women and decrease them in transgender men; more research is needed on migraine management in transgender individuals.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Personalized treatments for hair loss are becoming more effective by using genetic information.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.