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The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Genetic discoveries are leading to new treatments for alopecia areata.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

DNA analysis can help tailor alopecia treatment.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Researchers found 15 new genetic links to skin traits in Japanese women.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

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

Beetroot extract nanogel may help treat hair loss caused by testosterone.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

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

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Two siblings have a rare genetic condition causing curly, coarse hair.

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

The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

Boxer dogs may have a genetic skin condition that worsens seasonally and can be treated with certain medications.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

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.