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Different stages and types of female hair loss are linked with age, menopause, high blood pressure, and skin conditions like acne and hirsutism.

People with androgenetic alopecia, both men and women, are more likely to develop heart diseases in the future.

Substances from Ascidian tunics might help treat hair loss as effectively as Minoxidil.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Prunus mira kernels contain components that can promote hair growth in mice.

High YKL-40 levels predict early hair loss and hidden metabolic issues.

Hair loss, known as Androgenetic Alopecia, is often caused by hormones and can be diagnosed using noninvasive techniques. Treatments include topical minoxidil and oral finasteride, with new treatments being explored. There may also be a link between this type of hair loss and heart disease risk.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

Nanocarriers with plant extracts show promise for safe and effective hair growth treatment.

Different types of female pattern hair loss have unique characteristics and are associated with various health conditions.

Nourkrin® with Marilex® may significantly increase hair growth and alopecia could be an early sign of metabolic syndrome.

Smoking may worsen hair loss, but more research is needed.

Female pattern hair loss does not significantly affect sexual dysfunction.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

A girl had rickets due to a gene mutation affecting vitamin D response.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

An 18-year-old girl was diagnosed with a rare hereditary hair loss condition, despite no family history.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

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