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Autoimmune liver diseases are likely linked to certain skin conditions like vitiligo and psoriasis.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

The 2003 consensus updated PCOS diagnosis criteria and linked PCOS to higher risks of diabetes and heart problems, recommending lifestyle changes to lower these risks.

Premature balding in some men may be linked to altered hormones, but it's not the male equivalent to polycystic ovary syndrome or metabolic syndrome.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.

Low-dose acitretin helps nail psoriasis, stem cells may treat scarring alopecia, Chinese men have lower baldness rates, lateral foldplasty is good for ingrown toenails, hair diameter helps diagnose female baldness, childhood trauma linked to alopecia areata, certain hair-weaving leads to scalp conditions in African American women, and new methods for hair research and understanding hair and sweat gland development were introduced.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

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

Lipase H is important for hair follicle function and shaping hair fibers.

Different types of hair loss in dogs and cats have various causes and treatments, with outcomes ranging from good to uncertain.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Alopecia in animals can be hereditary, congenital, or acquired, with treatments and outcomes varying widely.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

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

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Premature graying of hair may suggest health issues and currently lacks effective treatments.

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

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.