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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Healthy mitochondria in skin cells are essential for proper hair growth and skin cell interaction in mice.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

Platelet-rich plasma (PRP) may help with various hair loss types, but more research is needed to find the best use method.

HLA-DRB5 and other genes may be linked to alopecia universalis.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Lower SMAD2/3 activation predicts more severe skin cancer.

Certain genes affect udder shape in Holstein cows, important for health and milk production.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Sex hormones' effects on COVID-19 are unclear and more research is needed to understand their potential as treatment.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

New genetic locations explain much of hair color variation in Europeans.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

Goats with BSE or scrapie show varying symptoms, and using only clinical signs may not detect all scrapie cases.

Low selenium levels can extend lifespan but worsen health issues.

Using low-dose IL-2 to increase regulatory T cells might be a safe way to treat type 1 diabetes without severe side effects.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

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

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Ethnic Indian women with PCOS often have early symptoms, delayed diagnosis, and need better information and support for treatment and lifestyle management.