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A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Lack of essential fatty acids in diet causes reproductive issues and poor health in male rabbits.

Woodhouse-Sakati Syndrome can include unique symptoms like liver issues and low growth hormone.

Iron therapy resolved uncooked rice cravings and symptoms in women with iron deficiency.

A woman's skin symptoms led to a diagnosis of systemic AL amyloidosis, but she died from sepsis shortly after.

New compounds were made that effectively block a specific enzyme related to androgen conditions.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Leucine levels may affect hair loss after bariatric surgery.

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

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Valproic acid can very rarely cause nail separation, which usually gets better on its own after stopping the drug.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Surgery successfully treated the ferret's adrenal issue, leading to hair regrowth and improved health.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Children with alopecia areata should only have thyroid screening if they have Down syndrome, a history of atopy, family history of thyroid disease, or signs of thyroid problems.

Insulin resistance may contribute to hair loss in people with androgenic alopecia.

A potential treatment for atopic dermatitis could be to increase PADI1 expression to improve skin barrier function.

Corin helps control salt and sweat release in sweat glands.

Adolescents with hair loss show different hormone levels by sex and often have related metabolic issues.

Low androgen levels can still cause female pattern hair loss.

Early diagnosis and treatment of myositis in SLE patients lead to positive outcomes.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

A Rathke's cleft cyst caused hormonal imbalances and symptoms in a 68-year-old woman.

A man's adrenal insufficiency was caused by a pituitary tumor linked to kidney cancer.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Higher methionine levels in pregnant rabbits' diets improve hair follicle development and hair fiber diameter in their babies.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.

Nitrogen starvation in microalgae increases lipid production, making it a potential biofuel source.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.